Q2 2026 AngioDynamics Inc Earnings Call
Speaker #2: This conference call is also being broadcast live over the internet in the Investors section of the company's website at www.angiodynamics.com.
Speaker #2: A webcast replay of the call will be available at the same site, approximately one hour after the end of today's call.
Speaker #2: we Before begin , I'd like to caution listeners that during the course of this conference call , the company will make projections or forward looking statements regarding future events , including about statements expected margins for gross fiscal revenue , earnings and adjusted year 2026 , as well as trends that may continue management encourages you to review the company's past and future filings with the SEC , including , without limitation , the company's Forms 10-K and 10-K , which identify specific factors that may cause the actual results or events to differ materially from those described in the forward looking statements .
Speaker #2: The company will also discuss certain non-GAAP and pro forma financial measures during this call. Management uses these measures to establish and review operational performance goals and believes that these measures may assist investors in analyzing the underlying trends in the company's business over time.
Speaker #2: Investors should forma these consider non-GAAP and measures . In to addition not as a for or as substitute superior to financial reporting measures in prepared accordance with GAAP .
Speaker #2: A slide package offering insight into the the also available in results is company's company's section of the under events and Presentations . This presentation should be read in conjunction with the press release discussing the company's operating results financial performance .
Operator: Before we begin, I'd like to caution listeners that during the course of this conference call, the company will make projections or forward-looking statements regarding future events, including statements about expected revenue, adjusted earnings, and gross margins for Q2, Q3, Q4, as well as trends that may continue. Management encourages you to review the company's past and future filings with the SEC, including, without limitation, the company's Forms 10-Q and 10-K, which identify specific factors that may cause the actual results or events to differ materially from those described in the forward-looking statements. The company will also discuss certain non-GAAP and pro forma financial measures during this call. Management uses these measures to establish operational goals and review operational performance and believes that these measures may assist investors in analyzing the underlying trends in the company's business over time.
Before we begin, I'd like to caution listeners that during the course of this conference call, the company will make projections or forward-looking statements regarding future events, including statements about expected revenue, adjusted earnings, and gross margins for Q2, Q3, Q4, as well as trends that may continue. Management encourages you to review the company's past and future filings with the SEC, including, without limitation, the company's Forms 10-Q and 10-K, which identify specific factors that may cause the actual results or events to differ materially from those described in the forward-looking statements. The company will also discuss certain non-GAAP and pro forma financial measures during this call. Management uses these measures to establish operational goals and review operational performance and believes that these measures may assist investors in analyzing the underlying trends in the company's business over time.
Speaker #2: And during this morning's conference call, unless otherwise noted, all metrics and growth rates mentioned during today's call are on a pro forma basis, which results from the dialysis and BioCentury businesses that were divested in June 2023.
Speaker #2: The PICC and midline products that were divested in February 2024, and the radio frequency and Syntrax support catheter products that we discontinued in February 2024.
Speaker #2: Also , unless otherwise noted , all comparisons will be the second fiscal quarter of 2026 versus the fiscal quarter of 2025 . Now , I'd like to turn the call over to Jim Clemmer , ANGIODYNAMICS INC President and Chief Executive Officer .
Speaker #2: Mr. Clemmer .
Speaker #3: Thank you . Operator . Good morning , everyone , and thank you for joining for Angiodynamics us fiscal 2026 second quarter earnings call .
Operator: Investors should consider these non-GAAP and pro forma measures in addition to, not as a substitute for or as superior to, financial reporting measures prepared in accordance with GAAP. A slide package offering insight into the company's financial results is also available in the investors' section of the company's website under events and presentations. This presentation should be read in conjunction with the press release discussing the company's operating results and financial performance during this morning's conference call. Unless otherwise noted, all metrics and growth rates mentioned during today's call are on a pro forma basis, which exclude the results of the dialysis and BioSentry businesses that were divested in June 2023, the PIC and Midline products that were divested in February 2024, and the radio frequency and Syntrax support catheter products that we discontinued in February 2024.
Investors should consider these non-GAAP and pro forma measures in addition to, not as a substitute for or as superior to, financial reporting measures prepared in accordance with GAAP. A slide package offering insight into the company's financial results is also available in the investors' section of the company's website under events and presentations. This presentation should be read in conjunction with the press release discussing the company's operating results and financial performance during this morning's conference call. Unless otherwise noted, all metrics and growth rates mentioned during today's call are on a pro forma basis, which exclude the results of the dialysis and BioSentry businesses that were divested in June 2023, the PIC and Midline products that were divested in February 2024, and the radio frequency and Syntrax support catheter products that we discontinued in February 2024.
Speaker #3: Joining me today is Steve Trowbridge, AngioDynamics Executive Vice President and Chief Financial Officer. We delivered strong results in the second quarter.
Speaker #3: Revenue grew 8.8%, with MedTech up 13%. And we translated that top-line performance into improved profitability. Adjusted EBITDA nearly doubled year over year.
Speaker #3: And we generated positive cash flow . These results prove that we can drive both revenue growth and profitability simultaneously Based . on our strong performance , we are raising our full year guidance for both revenue and adjusted EBITDA , which Steve will detail later in the call .
Operator: Also, unless otherwise noted, all comparisons will be the second fiscal quarter of 2026 versus the second fiscal quarter of 2025. Now, I'd like to turn the call over to Jim Clemmer, AngioDynamics' President and Chief Executive Officer. Mr. Clemmer? Thank you, Operator. Good morning, everyone, and thank you for joining us for AngioDynamics' Q2, Q2 earnings call. Joining me today is Steve Trowbridge, AngioDynamics Executive Vice President and Chief Financial Officer. We delivered strong results in the second quarter. Revenue grew 8.8%, with med tech up 13%, and we translated that top-line performance into improved profitability. Adjusted EBITDA nearly doubled year over year, and we generated positive cash flow. These results prove that we can drive both revenue growth and profitability simultaneously. Based on our strong performance, we are raising our full-year guidance for both revenue and adjusted EBITDA, which Steve will detail later in the call.
Also, unless otherwise noted, all comparisons will be the second fiscal quarter of 2026 versus the second fiscal quarter of 2025. Now, I'd like to turn the call over to Jim Clemmer, AngioDynamics' President and Chief Executive Officer. Mr. Clemmer?
Speaker #3: What's particularly encouraging is the breadth across our of our execution portfolio . delivered Rian another quarter digit year double of over year growth Our .
Jim Clemmer: Thank you, Operator. Good morning, everyone, and thank you for joining us for AngioDynamics' Q2, Q2 earnings call. Joining me today is Steve Trowbridge, AngioDynamics Executive Vice President and Chief Financial Officer. We delivered strong results in the second quarter. Revenue grew 8.8%, with med tech up 13%, and we translated that top-line performance into improved profitability. Adjusted EBITDA nearly doubled year over year, and we generated positive cash flow. These results prove that we can drive both revenue growth and profitability simultaneously. Based on our strong performance, we are raising our full-year guidance for both revenue and adjusted EBITDA, which Steve will detail later in the call.
Speaker #3: Mechanical thrombectomy platforms continue to gain traction, both commercially and from a regulatory product development standpoint. NanoKnife is well positioned to capitalize on the prostate opportunity, with the CPT code becoming effective a few days ago, and our med device business delivered solid results.
Speaker #3: let me Now , through walk you each of our businesses . Arion continues to perform exceptionally well . We delivered our 18th consecutive quarter of double digit growth , and we continue to take share in the Atherectomy market .
Speaker #3: Our strategy to increase penetration in hospitals is working, driving both higher volumes and better economics. International is starting to contribute, following our approval.
Operator: What's particularly encouraging is the breadth of our execution across our portfolio. Auryon delivered another quarter of double-digit year-over-year growth. Our mechanical thrombectomy platforms continue to gain traction, both commercially and from a regulatory product development standpoint. NanoKnife is well-positioned to capitalize on the prostate opportunity, with the CPT code becoming effective a few days ago, and our Med Device business delivered solid results. Now, let me walk you through each of our businesses. Auryon continues to perform exceptionally well. We delivered our 18th consecutive quarter of double-digit growth, and we continue to take share in the atherectomy market. Our strategy to increase penetration in hospitals is working, driving both higher volumes and better economics. International is starting to contribute following our CE Mark approval. We're also making progress on expanding the addressable market. The Ambition BTK study is enrolling well, and we're advancing our work towards coronary applications.
What's particularly encouraging is the breadth of our execution across our portfolio. Auryon delivered another quarter of double-digit year-over-year growth. Our mechanical thrombectomy platforms continue to gain traction, both commercially and from a regulatory product development standpoint. NanoKnife is well-positioned to capitalize on the prostate opportunity, with the CPT code becoming effective a few days ago, and our Med Device business delivered solid results. Now, let me walk you through each of our businesses. Auryon continues to perform exceptionally well. We delivered our 18th consecutive quarter of double-digit growth, and we continue to take share in the atherectomy market. Our strategy to increase penetration in hospitals is working, driving both higher volumes and better economics. International is starting to contribute following our CE Mark approval. We're also making progress on expanding the addressable market. The Ambition BTK study is enrolling well, and we're advancing our work towards coronary applications.
Speaker #3: We're also making progress on expanding the addressable market. The Ambition BTK study is enrolling well, and we're advancing our work towards coronary applications.
Speaker #3: These initiatives will take time , but they represent opportunities to broaden where Arion can compete . Moving to mechanical thrombectomy . We are pleased with the continued trajectory of our mechanical thrombectomy platform , and we are thrilled with the three regulatory milestones that we announced today in this portfolio .
Speaker #3: Our combined mechanical thrombectomy portfolio grew 3.9% over the prior year , driven by continued growth . addition , in In we performance continued with the are pleased of Angiovac Alpha VAC maintained its momentum , sequential delivering quarterly growth and strong year over year growth .
Speaker #3: This quarter, we continued to win new accounts, move through the hospital value analysis committees, and see strong physician feedback on the advantages of the unique design of our platform.
Speaker #3: was Angiovac down year over year this quarter , impacted by a tough comparison against a particularly strong second quarter in 2025 . We will continue to be excited about the trajectory of the business , and we remain in the long confident term opportunity ahead a from regulatory standpoint , we made significant progress this quarter with three important milestones for our mechanical thrombectomy portfolio that strengthen our competitive position and expand our clinical applications .
Operator: These initiatives will take time, but they represent opportunities to broaden where Auryon can compete. Moving to mechanical thrombectomy, we are pleased with the continued trajectory of our mechanical thrombectomy platform, and we are thrilled with the three regulatory milestones that we announced today in this portfolio. Our combined mechanical thrombectomy portfolio grew 3.9% over the prior year, driven by continued growth in AlphaVac. In addition, we are pleased with the continued performance of AngioVac. AlphaVac maintained its momentum, delivering sequential quarterly growth and strong year-over-year growth this quarter. We continue to win new accounts, move through the hospital value analysis committees, and see strong physician feedback on the unique design advantages of our platform. AngioVac was down year-over-year this quarter, impacted by a tough comparison against a particularly strong Q2 in 2025.
These initiatives will take time, but they represent opportunities to broaden where Auryon can compete. Moving to mechanical thrombectomy, we are pleased with the continued trajectory of our mechanical thrombectomy platform, and we are thrilled with the three regulatory milestones that we announced today in this portfolio. Our combined mechanical thrombectomy portfolio grew 3.9% over the prior year, driven by continued growth in AlphaVac. In addition, we are pleased with the continued performance of AngioVac. AlphaVac maintained its momentum, delivering sequential quarterly growth and strong year-over-year growth this quarter. We continue to win new accounts, move through the hospital value analysis committees, and see strong physician feedback on the unique design advantages of our platform. AngioVac was down year-over-year this quarter, impacted by a tough comparison against a particularly strong Q2 in 2025.
Speaker #3: First , we received I'd approval for our apex return study , a pivotal trial evaluating the Alpha return blood management system . When used with alpha vac treating for acute pulmonary embolism .
Speaker #3: Alpha return addresses a hurdle to initial adoption that a number of prospective new customers raised have , which is the ability to collect , filter , and aspirated reinfuse blood during thrombectomy procedures .
Speaker #3: We believe that this additional offering will be a to catalyst accelerating the already impressive growth profile of Alpha VAC . Second , we received IDE Pave for our , a study pilot trial evaluating Angiovac for the percutaneous removal of right heart vegetation in patients with right sided infective endocarditis .
Operator: We will continue to be excited about the trajectory of the business, and we remain confident in the long-term opportunity ahead. From a regulatory standpoint, we made significant progress this quarter with three important milestones for our mechanical thrombectomy portfolio that strengthen our competitive position and expand our clinical applications. First, we received IDE approval for our APEX-Return study, a pivotal trial evaluating the AlphaReturn blood management system when used with AlphaVac for treating acute pulmonary embolism. AlphaReturn addresses a hurdle to initial adoption that a number of prospective new customers have raised, which is the ability to collect, filter, and reinfuse aspirated blood during thrombectomy procedures. We believe that this additional offering will be a catalyst to accelerating the already impressive growth profile of AlphaVac.
We will continue to be excited about the trajectory of the business, and we remain confident in the long-term opportunity ahead. From a regulatory standpoint, we made significant progress this quarter with three important milestones for our mechanical thrombectomy portfolio that strengthen our competitive position and expand our clinical applications. First, we received IDE approval for our APEX-Return study, a pivotal trial evaluating the AlphaReturn blood management system when used with AlphaVac for treating acute pulmonary embolism. AlphaReturn addresses a hurdle to initial adoption that a number of prospective new customers have raised, which is the ability to collect, filter, and reinfuse aspirated blood during thrombectomy procedures. We believe that this additional offering will be a catalyst to accelerating the already impressive growth profile of AlphaVac.
Speaker #3: This addresses and underserved patient limited population with treatment options , particularly when surgical risk is high . Third , received 510 K we for a modified alpha vac F-18 85 system with expanded indications .
Speaker #3: The clearance expands the cannula indication to allow aspiration and injection of contrast media and other fluids, and includes the sheath as an alternative introducer that minimizes blood loss.
Speaker #3: These enhancements give physicians greater flexibility in how they use the device across a broader range of cases. Together, these regulatory wins demonstrate the strength of our innovation and our mechanical thrombectomy platform.
Operator: Second, we received IDE approval for our PAVE study, a pilot trial evaluating AngioVac for the percutaneous removal of right heart vegetation in patients with right-sided infective endocarditis. This addresses an underserved patient population with limited treatment options, particularly when surgical risk is high. Third, we received 510(k) clearance for a modified AlphaVac F1885 system with expanded indications. The clearance expands the cannula indication to allow aspiration and injection of contrast media and other fluids and includes the sheath as an alternative introducer that minimizes blood loss. These enhancements give physicians greater flexibility in how they use the device across a broader range of cases. Together, these regulatory wins demonstrate the versatility and innovation of our mechanical thrombectomy platform.
Second, we received IDE approval for our PAVE study, a pilot trial evaluating AngioVac for the percutaneous removal of right heart vegetation in patients with right-sided infective endocarditis. This addresses an underserved patient population with limited treatment options, particularly when surgical risk is high. Third, we received 510(k) clearance for a modified AlphaVac F1885 system with expanded indications. The clearance expands the cannula indication to allow aspiration and injection of contrast media and other fluids and includes the sheath as an alternative introducer that minimizes blood loss. These enhancements give physicians greater flexibility in how they use the device across a broader range of cases. Together, these regulatory wins demonstrate the versatility and innovation of our mechanical thrombectomy platform.
Speaker #3: They represent meaningful opportunities to expand clinical applications, address unmet patient needs, and strengthen our competitive position in the thrombectomy market by delivering improved treatment options that physicians are seeking to improve patient outcomes.
Speaker #3: NanoKnife delivered strong growth this quarter, driven by prostate procedures. The CPT code went live on January 1st, which should provide a tailwind for adoption.
Speaker #3: We've been consistent in our messaging that this adoption will build over time, rather than be an immediate step change, and that's what we're seeing.
Speaker #3: interest is high Physician volumes are procedure growing , and we are executing on our commercial and awareness building initiatives . We believe we're well positioned as this market develop Finally , in continues to .
Speaker #3: In October, we were excited that the NanoKnife system was named to TIME's 2025 Best Innovations list, which we believe will accelerate patient awareness in this growing market.
Operator: They represent meaningful opportunities to expand clinical applications, address unmet patient needs, and strengthen our competitive position in the thrombectomy market by delivering improved treatment options that physicians are seeking to improve patient outcomes. NanoKnife delivered strong growth this quarter, driven by prostate procedures. The CPT code went live on 1 January, which should provide a tailwind for adoption. We've been consistent in our messaging that this adoption will build over time rather than be an immediate step change, and that's what we're seeing. Physician interest is high, procedure volumes are growing, and we are executing on our commercial and awareness-building initiatives. We believe we're well-positioned as this market continues to develop. Finally, in October, we were excited that the NanoKnife system was named to TIME's 2025 Best Inventions list, which we believe will accelerate patient awareness in this growing market.
They represent meaningful opportunities to expand clinical applications, address unmet patient needs, and strengthen our competitive position in the thrombectomy market by delivering improved treatment options that physicians are seeking to improve patient outcomes. NanoKnife delivered strong growth this quarter, driven by prostate procedures. The CPT code went live on 1 January, which should provide a tailwind for adoption. We've been consistent in our messaging that this adoption will build over time rather than be an immediate step change, and that's what we're seeing. Physician interest is high, procedure volumes are growing, and we are executing on our commercial and awareness-building initiatives. We believe we're well-positioned as this market continues to develop. Finally, in October, we were excited that the NanoKnife system was named to TIME's 2025 Best Inventions list, which we believe will accelerate patient awareness in this growing market.
Speaker #3: Med device grew over 5% this quarter, ahead of our expectations. The team running this business executes consistently, and it provides profitable cash flow that supports our medtech investments.
Speaker #3: at the Looking quarter we're executing on overall , multiple fronts . We grew revenue , expanded margins advanced important . We clinical programs , and we generated cash .
Speaker #3: Our first half performance gives us confidence in our ability to operate efficiently while investing in the initiatives that position us for sustained growth. That balance—growth between delivering today and investing for tomorrow—is what will drive long-term value creation.
Speaker #3: Now, let me turn the call to Steve for the financial details. Thanks, Jim.
Speaker #4: And good morning , everybody . As always , before I begin , I'd like to direct everyone to the presentation on our Investor Relations website summarizing the key items from our quarterly results .
Speaker #4: Unless otherwise noted, all metrics and growth rates mentioned during today's call are on a pro forma basis, which exclude the results of the Dialysis and BioCentury businesses that we divested in June 2023.
Operator: Med Device grew over 5% this quarter, ahead of our expectations. The team running this business executes consistently, and it provides profitable cash flow that supports our Med Tech investments. Looking at the quarter overall, we're executing on multiple fronts. We grew revenue, expanded margins, advanced important clinical programs, and generated cash. Our first-half performance gives us confidence in our ability to operate efficiently while investing in the initiatives that position us for sustained growth. That balance between delivering today and investing for tomorrow is what will drive long-term value creation. Now, let me turn the call to Steve for the financial details. Thanks, Jim. And good morning, everybody. As always, before I begin, I'd like to direct everyone to the presentation on our investor relations website summarizing the key items from our quarterly results.
Med Device grew over 5% this quarter, ahead of our expectations. The team running this business executes consistently, and it provides profitable cash flow that supports our Med Tech investments. Looking at the quarter overall, we're executing on multiple fronts. We grew revenue, expanded margins, advanced important clinical programs, and generated cash. Our first-half performance gives us confidence in our ability to operate efficiently while investing in the initiatives that position us for sustained growth. That balance between delivering today and investing for tomorrow is what will drive long-term value creation. Now, let me turn the call to Steve for the financial details.
Speaker #4: The PIC and midline products that we divested in February 2024, and the radio and Syntrax support catheter products that we discontinued also in February 2024.
Speaker #4: Additionally, unless otherwise noted, all comparisons will be the second fiscal quarter of 2026 versus the second fiscal quarter of 2025. Top line revenue performance in the increased quarter.
Speaker #4: Revenue was strong again, up 8.8% to $79.4 million, with growth driven across both our MedTech and Med Device segments. Revenue from MedTech was $35.7 million, a 13% increase.
Speaker #4: We're very pleased with the performance of our MedTech segment. Now, the comp for our second quarter was much more difficult than the comp for our first quarter, and year to date, MedTech is up 19.1% in the quarter.
Steve Trowbridge: Thanks, Jim. And good morning, everybody. As always, before I begin, I'd like to direct everyone to the presentation on our investor relations website summarizing the key items from our quarterly results.
Speaker #4: Our Med Device revenue was $43.8 million, an increase of 5.6% for the second fiscal quarter. Our MedTech platforms comprised 45% of our total revenue, compared to 43% of total revenue a year ago.
Operator: Unless otherwise noted, all metrics and growth rates mentioned during today's call are on a pro forma basis, which exclude the results of the dialysis and BioSentry businesses that we divested in June 2023, the PICC and Midline products that we divested in February 2024, and the radio frequency and Syntrax support catheter products that we discontinued also in February 2024. Additionally, unless otherwise noted, all comparisons will be the second fiscal quarter of 2026 versus the second fiscal quarter of 2025. Top-line revenue performance was strong again in the quarter. Revenue increased 8.8% to $79.4 million, driven by growth across both our Med Tech and Med Device segments. Med Tech revenue was $35.7 million, a 13% increase. We're very pleased with the performance of our Med Tech segment. Now, the comp for our second quarter was much more difficult than the comp for our first quarter.
Unless otherwise noted, all metrics and growth rates mentioned during today's call are on a pro forma basis, which exclude the results of the dialysis and BioSentry businesses that we divested in June 2023, the PICC and Midline products that we divested in February 2024, and the radio frequency and Syntrax support catheter products that we discontinued also in February 2024. Additionally, unless otherwise noted, all comparisons will be the second fiscal quarter of 2026 versus the second fiscal quarter of 2025. Top-line revenue performance was strong again in the quarter. Revenue increased 8.8% to $79.4 million, driven by growth across both our Med Tech and Med Device segments. Med Tech revenue was $35.7 million, a 13% increase. We're very pleased with the performance of our Med Tech segment. Now, the comp for our second quarter was much more difficult than the comp for our first quarter.
Speaker #4: Further illustrating the sustained execution of our strategy to increase the percentage of our overall base revenue coming from our higher-growth, higher-margin MedTech segment.
Speaker #4: our Digging into medtech segment , our Orion platform contributed 16.3 million in revenue , growing 18.6% compared to last year . Orion has now delivered double digit year over year growth for 18 consecutive quarters .
Speaker #4: As Jim mentioned, this growth is supported by our strategy to increase the percentage of our atherectomy business in the hospital side of care.
Speaker #4: In addition to this mix shift, we continue to grow our customer base in both the hospital and OB settings, and are benefiting from continued adoption following internationally.
Speaker #4: CE Mark approval in September of last year, mechanical thrombectomy revenue, which includes AngioVac and AlphaVac sales, increased 3.9% year over year with revenue of $11 million in the quarter.
Operator: Year to date, Med Tech is up 19.1%. In the quarter, our Med Device revenue was $43.8 million, an increase of 5.6%. For the second fiscal quarter, our Med Tech platforms comprised 45% of our total revenue compared to 43% of total revenue a year ago, further illustrating the sustained execution of our strategy to increase the percentage of our overall revenue base coming from our higher growth, higher margin Med Tech segment. Digging into our Med Tech segment, our Auryon platform contributed $16.3 million in revenue, growing 18.6% compared to last year. Auryon has now delivered double-digit year-over-year growth for 18 consecutive quarters. As Jim mentioned, this growth is supported by our strategy to increase the percentage of our atherectomy business in the hospital site of care.
Year to date, Med Tech is up 19.1%. In the quarter, our Med Device revenue was $43.8 million, an increase of 5.6%. For the second fiscal quarter, our Med Tech platforms comprised 45% of our total revenue compared to 43% of total revenue a year ago, further illustrating the sustained execution of our strategy to increase the percentage of our overall revenue base coming from our higher growth, higher margin Med Tech segment. Digging into our Med Tech segment, our Auryon platform contributed $16.3 million in revenue, growing 18.6% compared to last year. Auryon has now delivered double-digit year-over-year growth for 18 consecutive quarters. As Jim mentioned, this growth is supported by our strategy to increase the percentage of our atherectomy business in the hospital site of care.
Speaker #4: Angiovac revenue was 7.5 million , a 7.5% year over year decrease in Alphavax revenue was 3.5 million , a 40.2% year over year increase , while Angiovac revenue was down year over year .
Speaker #4: pleased with the continued We strength in this business , which delivered year to date growth of 11.2% , Q2 of last year exhibited the initial in Angiovac step up revenue and therefore provided for a tough comp .
Speaker #4: We remain bullish on AngioVac going forward and are encouraged by the particularly sustained procedure volumes for this product. The approval of our IDE to study the use of AngioVac to treat right-sided infective endocarditis will be an enabler of sustained growth for AngioVac in the future.
Speaker #4: VAC Alpha continued its sequential quarter-over-quarter growth, and as Jim mentioned, the approval of our IDE for our blood return product will be an additional catalyst to accelerate momentum in Alpha Vac.
Operator: In addition to this mixed shift, we continue to grow our customer base in both the hospital and OBL settings and are benefiting from continued adoption internationally following CE Mark approval in September of last year. Mechanical thrombectomy revenue, which includes AngioVac and AlphaVac sales, increased 3.9% year-over-year with revenue of $11 million. In the quarter, AngioVac revenue was $7.5 million, a 7.5% year-over-year decrease, and AlphaVac revenue was $3.5 million, a 40.2% year-over-year increase. While AngioVac revenue was down year-over-year, we are pleased with the continued strength in this business, which delivered year-to-date growth of 11.2%. Q2 of last year exhibited the initial step-up in AngioVac revenue and therefore provided for a tough comp. We remain bullish on AngioVac going forward and are particularly encouraged by the sustained procedure volumes for this product.
In addition to this mixed shift, we continue to grow our customer base in both the hospital and OBL settings and are benefiting from continued adoption internationally following CE Mark approval in September of last year. Mechanical thrombectomy revenue, which includes AngioVac and AlphaVac sales, increased 3.9% year-over-year with revenue of $11 million. In the quarter, AngioVac revenue was $7.5 million, a 7.5% year-over-year decrease, and AlphaVac revenue was $3.5 million, a 40.2% year-over-year increase. While AngioVac revenue was down year-over-year, we are pleased with the continued strength in this business, which delivered year-to-date growth of 11.2%. Q2 of last year exhibited the initial step-up in AngioVac revenue and therefore provided for a tough comp. We remain bullish on AngioVac going forward and are particularly encouraged by the sustained procedure volumes for this product.
Speaker #4: Mechanical combined thrombectomy portfolio continues to demonstrate strong momentum with our teams, effectively positioning sales of AngioVac and AlphaVac based on clinical need and physician preference.
Speaker #4: Total Nanoknife revenue was an increase of 22.2% , with probe growth of 14.4% . Probe growth continues to be driven by increasing growth in demand and utilization of Nanoknife to treat prostate cancer patients in Q2 was a quarter for record us for prostate procedure cases .
Speaker #4: Sales were transactions in France in which we moved from a direct sales model to a distribution model. As part of this transaction, the new distribution partner purchased NanoKnife systems that were previously placed at customer sites and were included on our balance sheet.
Operator: The approval of our IDE to study the use of AngioVac to treat right-sided infective endocarditis will be an enabler of sustained growth for AngioVac in the future. AlphaVac continued its sequential quarter-over-quarter growth, and as Jim mentioned, the approval of our IDE for our blood return product will be an additional catalyst to accelerate momentum in AlphaVac. Combined mechanical thrombectomy portfolio continues to demonstrate strong momentum, with our sales teams effectively positioning both AngioVac and AlphaVac based on clinical need and physician preference. Total NanoKnife revenue was $7.3 million, an increase of 22.2%, with probe growth of 14.4%. Probe growth continues to be driven by increasing growth in demand and utilization of NanoKnife to treat prostate cancer patients, and Q2 was a record quarter for us for prostate procedure cases.
The approval of our IDE to study the use of AngioVac to treat right-sided infective endocarditis will be an enabler of sustained growth for AngioVac in the future. AlphaVac continued its sequential quarter-over-quarter growth, and as Jim mentioned, the approval of our IDE for our blood return product will be an additional catalyst to accelerate momentum in AlphaVac. Combined mechanical thrombectomy portfolio continues to demonstrate strong momentum, with our sales teams effectively positioning both AngioVac and AlphaVac based on clinical need and physician preference. Total NanoKnife revenue was $7.3 million, an increase of 22.2%, with probe growth of 14.4%. Probe growth continues to be driven by increasing growth in demand and utilization of NanoKnife to treat prostate cancer patients, and Q2 was a record quarter for us for prostate procedure cases.
Speaker #4: In addition to NanoKnife sales, this transaction also included Orion Microwave and EVLT capital sales. NanoKnife capital sales in the transaction were approximately $1 million, and Microwave and EVLT capital sales were approximately $250,000 each.
Speaker #4: This represents a smart transaction that will enable growth in a strategic international market. I applaud the efforts of our international team, and specifically Laura Piccinini, our GM of Global Cardiovascular and International.
Speaker #4: For executing on deal this . In the second quarter , our med device segment increased 5.6% year over year . date , our A year to med device segment is up 4% .
Speaker #4: We are very pleased with the performance of this segment, and while we do not expect our Med Device growth at this segment to be at this high a level for the full year—which I will discuss in more detail in a moment—we are raising our expectations for Med Device for the full year, up from our previous guidance to the income.
Operator: NanoKnife capital sales were bolstered by a transaction in France in which we moved from a direct sales model to a distribution model. As part of this transaction, the new distribution partner purchased NanoKnife systems that were previously placed at customer sites and were included on our balance sheet. In addition to NanoKnife sales, this transaction also included Auryon, Microwave, and EVLT capital sales. NanoKnife capital sales in the transaction were approximately $1 million, and Auryon, Microwave, and EVLT capital sales were approximately $250,000 each. Now, this represents a smart transaction that will enable growth in a strategic international market. I applaud the efforts of our international team and specifically Laura Piccinini, our GM of Global Cardiovascular International, for executing on this deal. In Q2, our Med Device segment increased 5.6% year-over-year. Year to date, our Med Device segment is up 4%.
NanoKnife capital sales were bolstered by a transaction in France in which we moved from a direct sales model to a distribution model. As part of this transaction, the new distribution partner purchased NanoKnife systems that were previously placed at customer sites and were included on our balance sheet. In addition to NanoKnife sales, this transaction also included Auryon, Microwave, and EVLT capital sales. NanoKnife capital sales in the transaction were approximately $1 million, and Auryon, Microwave, and EVLT capital sales were approximately $250,000 each. Now, this represents a smart transaction that will enable growth in a strategic international market. I applaud the efforts of our international team and specifically Laura Piccinini, our GM of Global Cardiovascular International, for executing on this deal. In Q2, our Med Device segment increased 5.6% year-over-year. Year to date, our Med Device segment is up 4%.
Speaker #4: Our moving down gross now margin for the second quarter of FY26 was 56.4%, a 170 basis point increase from fiscal 2025.
Speaker #4: The year over year improvement was driven by product mix continued shift towards med tech sales , accelerated benefits from our manufacturing transfer initiatives , and the sales channel transaction in France .
Speaker #4: Manufacturing transfer with respect to the initiative, our operations team has done a fantastic job executing on our manufacturing optimization strategy, and we have been able to accelerate a meaningful portion of cost savings ahead of schedule.
Speaker #4: briefly on Touching tariffs . The expense in Q2 was in line with our expectations . And as we discussed last quarter , we continue to expect to incur between 4 and 6 million of tariff expenses for the full fiscal year 2026 .
Speaker #4: Total operating expenses in the quarter were $50.9 million, down to 64.1% of sales, compared to $51 million, or 69.9% of sales last year.
Operator: We are very pleased with the performance of this segment, and while we do not expect our med device segment to grow at this level for the full year, as I will discuss in more detail in a moment, we are raising our expectations for med device for the full year up from our previous guidance. Now, moving down the income statement, our gross margin for the second quarter of FY26 was 56.4%, a 170 basis point increase from the second quarter of fiscal year 2025. The year-over-year improvement was driven by continued product mix shift towards med tech sales, accelerated benefits from our manufacturing transfer initiatives, and the sales channel transaction in France.
We are very pleased with the performance of this segment, and while we do not expect our med device segment to grow at this level for the full year, as I will discuss in more detail in a moment, we are raising our expectations for med device for the full year up from our previous guidance. Now, moving down the income statement, our gross margin for the second quarter of FY26 was 56.4%, a 170 basis point increase from the second quarter of fiscal year 2025. The year-over-year improvement was driven by continued product mix shift towards med tech sales, accelerated benefits from our manufacturing transfer initiatives, and the sales channel transaction in France.
Speaker #4: we As continue to drive operating the business leverage in . Turning to R&D , our research and development expense was 7.8 million , or 9.8% of sales , compared to 6.4 million , or 8.8% of sales a year ago .
Speaker #4: Previously mentioned, we remain committed to investing in R&D initiatives to support the long-term growth of our medtech segment and are targeting approximately 10% of sales going forward.
Speaker #4: initiatives that Clinical we previously including the Ides for mentioned , Blood Return and Infective endocarditis treated with Angiovac , are included in our projections for the balance of the year , SG&A expense for the second quarter of FY 26 was $36.9 million , representing 46.4% of sales , compared to 36 million of 49.3% of sales a year ago .
Operator: With respect to our manufacturing transfer initiative, our operations team has done a fantastic job executing on our manufacturing optimization strategy, and we have been able to accelerate a meaningful portion of the cost savings ahead of schedule. Touching briefly on tariffs, the expense in Q2 was in line with our expectations, and as we discussed last quarter, we continue to expect to incur between $4 and 6 million of tariff expenses for the full fiscal year 2026. Total operating expenses in the quarter were $50.9 million, down to 64.1% of sales, compared to $51 million or 69.9% of sales last year as we continue to drive operating leverage in the business. Turning to R&D, our research and development expense was $7.8 million or 9.8% of sales compared to $6.4 million or 8.8% of sales a year ago.
With respect to our manufacturing transfer initiative, our operations team has done a fantastic job executing on our manufacturing optimization strategy, and we have been able to accelerate a meaningful portion of the cost savings ahead of schedule. Touching briefly on tariffs, the expense in Q2 was in line with our expectations, and as we discussed last quarter, we continue to expect to incur between $4 and 6 million of tariff expenses for the full fiscal year 2026. Total operating expenses in the quarter were $50.9 million, down to 64.1% of sales, compared to $51 million or 69.9% of sales last year as we continue to drive operating leverage in the business. Turning to R&D, our research and development expense was $7.8 million or 9.8% of sales compared to $6.4 million or 8.8% of sales a year ago.
Speaker #4: Our adjusted loss for the net second quarter of FY 26 was 0.1 million , or an adjusted loss per share of one tenth of a cent , compared to an adjusted net loss of 1.7 million , or an adjusted loss per share of $0.04 in the second quarter of last year .
Speaker #4: This year-over-year improvement is largely attributable to our MedTech revenue growth and the success of our gross margin initiatives and operating efficiencies.
Speaker #4: Adjusted EBITDA in the second quarter of FY26 was $5.9 million, compared to an adjusted EBITDA of $3.1 million in the second quarter of 2025.
Speaker #4: The France distribution transaction I discussed earlier contributed approximately 1.4 million of adjusted EBITDA in the quarter . We are very pleased with the adjusted EBITDA generation in the quarter , both including and excluding the fans transaction at 30 2025 , we had 41.6 million in cash and cash equivalents , compared to 38.8 million in cash and cash equivalents at August 31st , 2025 .
Operator: As previously mentioned, we remain committed to investing in R&D initiatives to support the long-term growth of our Med Tech segment and are targeting approximately 10% of sales going forward. Clinical initiatives that we previously mentioned, including the IDEs for blood return, and infective endocarditis treated with AngioVac, are included in our projections for the balance of the year. SG&A expense for Q2 FY26 was $36.9 million, representing 46.4% of sales, compared to $36 million or 49.3% of sales a year ago. Our adjusted net loss for Q2 FY26 was $0.1 million, or an adjusted loss per share of $0.001, compared to an adjusted net loss of $1.7 million or an adjusted loss per share of $0.04 in Q2 of last year.
As previously mentioned, we remain committed to investing in R&D initiatives to support the long-term growth of our Med Tech segment and are targeting approximately 10% of sales going forward. Clinical initiatives that we previously mentioned, including the IDEs for blood return, and infective endocarditis treated with AngioVac, are included in our projections for the balance of the year. SG&A expense for Q2 FY26 was $36.9 million, representing 46.4% of sales, compared to $36 million or 49.3% of sales a year ago. Our adjusted net loss for Q2 FY26 was $0.1 million, or an adjusted loss per share of $0.001, compared to an adjusted net loss of $1.7 million or an adjusted loss per share of $0.04 in Q2 of last year.
Speaker #4: In the second quarter of fiscal 26 , the company generated $4.7 million of cash , company's ahead of the expectations . We continue to expect to be cash flow positive for the full fiscal year 2026 , following the strong cash generation in the second fiscal quarter , we expect to utilize between 3 and 5 million of cash in the third quarter and then generate substantial cash in the fourth fiscal quarter , in line with historical trends .
Operator: This year-over-year improvement is largely attributable to our Med Tech revenue growth and the success of our gross margin initiatives, and operating efficiencies. Adjusted EBITDA in the second quarter of FY26 was $5.9 million compared to an adjusted EBITDA of $3.1 million in the second quarter of 2025. The France distribution transaction I discussed earlier contributed approximately $1.4 million of adjusted EBITDA in the quarter. We are very pleased with the adjusted EBITDA generation in the quarter, both including and excluding the France transaction. At 30 November 2025, we had $41.6 million in cash and cash equivalents compared to $38.8 million in cash and cash equivalents at 31 August 2025. In the second quarter of fiscal 26, the company generated $4.7 million of cash ahead of the company's expectations. We continue to expect to be cash flow positive for the full fiscal year 2026.
This year-over-year improvement is largely attributable to our Med Tech revenue growth and the success of our gross margin initiatives, and operating efficiencies. Adjusted EBITDA in the second quarter of FY26 was $5.9 million compared to an adjusted EBITDA of $3.1 million in the second quarter of 2025. The France distribution transaction I discussed earlier contributed approximately $1.4 million of adjusted EBITDA in the quarter. We are very pleased with the adjusted EBITDA generation in the quarter, both including and excluding the France transaction. At 30 November 2025, we had $41.6 million in cash and cash equivalents compared to $38.8 million in cash and cash equivalents at 31 August 2025. In the second quarter of fiscal 26, the company generated $4.7 million of cash ahead of the company's expectations. We continue to expect to be cash flow positive for the full fiscal year 2026.
Speaker #4: Turning now to guidance, based on our strong second quarter performance and our expectations for the balance of the year, we are raising components of our full-year fiscal 2026 guidance.
Speaker #4: We now expect net sales to be in the range of $312 million to $314 million, raised from our previously issued range of $308 million to $313 million.
Speaker #4: This increased range represents growth of between 6.6% and 7.3% over fiscal 2025 . Revenue of 292.7 million on a segment basis , we continue to expect medtech net sales to grow 14 to 16% , and we now expect med device sales to grow 0 to 1% , an increase from our prior guidance of flat growth .
Speaker #4: For fiscal 26 . We continue to expect gross margin to be in the range of 53.5% to 55.5% . This is inclusive of our reiterated estimate of impact for the 4 to 6 million of year full tariff we've mentioned , .
Operator: Following the strong cash generation in the second fiscal quarter, we expect to utilize between $3 and 5 million of cash in the third quarter and then generate substantial cash in the fourth fiscal quarter, in line with historical trends. Turning now to guidance. Based on our strong second quarter performance and our expectations for the balance of the year, we are raising components of our full year fiscal 2026 guidance. We now expect net sales to be in the range of $312 to 314 million, raised from our previously issued range of $308 to 313 million. This increased range represents growth of between 6.6% and 7.3% over fiscal 2025 revenue of $292.7 million.
Operator: Following the strong cash generation in the second fiscal quarter, we expect to utilize between $3 and 5 million of cash in the third quarter and then generate substantial cash in the fourth fiscal quarter, in line with historical trends. Turning now to guidance. Based on our strong second quarter performance and our expectations for the balance of the year, we are raising components of our full year fiscal 2026 guidance. We now expect net sales to be in the range of $312 to 314 million, raised from our previously issued range of $308 to 313 million. This increased range represents growth of between 6.6% and 7.3% over fiscal 2025 revenue of $292.7 million.
Speaker #4: As I accelerated some of the margin improvement initiatives during the first half of this fiscal year, we don't expect to see a significant step up in gross margin during the balance of the year.
Speaker #4: We now have EBITDA adjusted to be in the range of $8 million to $10 million, up from prior guidance of $6 million to $10 million.
Speaker #4: Again, inclusive of our pleased tariff, continue to be estimated. We impact about our ability to generate increasing adjusted EBITDA while accelerating investments into initiatives to support the long-term growth effectiveness of business, our which speaks to the overall strategy.
Speaker #4: Reminder, adjusted As a EBITDA will be lower in the second half of the year than it was in the first half, as our planned investments hit the P&L development.
Operator: On a segment basis, we continue to expect Med Tech net sales to grow 14% to 16%, and we now expect Med Device sales to grow 0% to 1% and increase from our prior guidance of flat growth. For fiscal 2026, we continue to expect gross margin to be in the range of 53.5% to 55.5%. This is inclusive of our reiterated estimate of $4 to 6 million of tariff impact for the full year. As I mentioned, we've accelerated some of our gross margin improvement initiatives during the first half of this fiscal year, so we don't expect to see a significant step-up in gross margin during the balance of the year. We now expect Adjusted EBITDA to be in the range of $8 to 10 million, up from prior guidance of $6 to 10 million, again inclusive of our estimated tariff impact.
On a segment basis, we continue to expect Med Tech net sales to grow 14% to 16%, and we now expect Med Device sales to grow 0% to 1% and increase from our prior guidance of flat growth. For fiscal 2026, we continue to expect gross margin to be in the range of 53.5% to 55.5%. This is inclusive of our reiterated estimate of $4 to 6 million of tariff impact for the full year. As I mentioned, we've accelerated some of our gross margin improvement initiatives during the first half of this fiscal year, so we don't expect to see a significant step-up in gross margin during the balance of the year. We now expect Adjusted EBITDA to be in the range of $8 to 10 million, up from prior guidance of $6 to 10 million, again inclusive of our estimated tariff impact.
Speaker #4: And finally, we continue to expect adjusted loss per share in the range of -$0.33 to -$0.23, unchanged from our prior guidance.
Speaker #4: pleased with our We're second quarter performance and the momentum we're building across the business . Our raised guidance reflects confidence in our ability to deliver sustained , profitable growth .
Speaker #4: Ending, I before want to briefly mention that following the quarter, we received notice that the US Court of Appeals for the Federal Circuit affirmed the district court's judgment in our previously settled patent litigation with C.R.
Speaker #4: Bard, invalidating Bard's patents. This decision concludes C.R. Bard's appeal and eliminates the potential that Angio would make a $3 million payment under the settlement agreement.
Speaker #4: This brings to a close litigation that we've successfully defended for more than a decade now. With that, I'll turn the call back to Jim.
Operator: We continue to be pleased about our ability to generate increasing Adjusted EBITDA while accelerating investments into initiatives to support the long-term growth of our business, which speaks to the effectiveness of our overall strategy. As a reminder, Adjusted EBITDA will be lower in the second half of the year than it was in the first half as our planned investments in clinical data development hit the P&L. Finally, we continue to expect adjusted loss per share in the range of negative $0.33 to negative $0.23, unchanged from our prior guidance. We're pleased with our second quarter performance and the momentum we're building across the business. Our raised guidance reflects confidence in our ability to deliver sustained, profitable growth. Before ending, I want to briefly mention that following the quarter, we received notice that the US.
We continue to be pleased about our ability to generate increasing Adjusted EBITDA while accelerating investments into initiatives to support the long-term growth of our business, which speaks to the effectiveness of our overall strategy. As a reminder, Adjusted EBITDA will be lower in the second half of the year than it was in the first half as our planned investments in clinical data development hit the P&L. Finally, we continue to expect adjusted loss per share in the range of negative $0.33 to negative $0.23, unchanged from our prior guidance. We're pleased with our second quarter performance and the momentum we're building across the business. Our raised guidance reflects confidence in our ability to deliver sustained, profitable growth. Before ending, I want to briefly mention that following the quarter, we received notice that the US.
Speaker #3: Before we open the line for questions . I want to share an update on the leadership transition . We announced earlier today . After a decade with the company , I have announced my intention to retire .
Speaker #3: I have spent over 30 years in the industry and have made the decision, along with my family, to move on to the next chapter of my life.
Speaker #3: The last ten years at AngioDynamics have been tremendously rewarding as we have transformed the company into a leading innovator of novel solutions that directly address the world's causes of two leading deaths.
Speaker #3: Within our medtech segment, we now have products addressing over a $10 billion global addressable market, and we have set ourselves up to be a physician partner and focus on expanding the applicability of these platforms to help more healthcare providers and their patients.
Operator: Court of Appeals for the Fed Circuit affirmed the district court's judgment in our previously settled port patent litigation with C. R. Bard, invalidating Bard's patents. This decision concludes C. R. Bard's appeal and eliminates the potential that ANGIO would make a $3 million payment under the settlement agreement. This brings to a close litigation that we've successfully defended for more than a decade. Now, with that, I'll turn the call back to Jim. Before we open the line for questions, I want to share an update on the leadership transition we announced earlier today. After a decade with the company, I have announced my intention to retire. I have spent over 30 years in the industry and have made the decision, along with my family, to move on to the next chapter of my life.
Court of Appeals for the Fed Circuit affirmed the district court's judgment in our previously settled port patent litigation with C. R. Bard, invalidating Bard's patents. This decision concludes C. R. Bard's appeal and eliminates the potential that ANGIO would make a $3 million payment under the settlement agreement. This brings to a close litigation that we've successfully defended for more than a decade. Now, with that, I'll turn the call back to Jim.
Speaker #3: With all of the work we have done, particularly over the last few years, the organization has earned enormous trust through the efficacy of our life-changing platforms, and we are in a fantastic position to execute on our strategy and momentum we continue to have built with the board.
Jim Clemmer: Before we open the line for questions, I want to share an update on the leadership transition we announced earlier today. After a decade with the company, I have announced my intention to retire. I have spent over 30 years in the industry and have made the decision, along with my family, to move on to the next chapter of my life.
Speaker #3: with the regard to the I worked timing of my retirement and the board has established a search committee is and conducting a comprehensive process , assisted by a leading executive search firm , to identify our next CEO , which we expect to occur during fiscal 2027 .
Operator: The last 10 years at AngioDynamics have been tremendously rewarding as we have transformed the company into a leading innovator of novel solutions that directly address the world's two leading causes of death. Within our med tech segment, we now have products addressing over a $10 billion global addressable market, and we have set ourselves up to be a physician partner and focus on expanding the applicability of these platforms to help more healthcare providers and their patients. With all of the work we have done, particularly over the last few years, the organization has earned enormous trust through the efficacy of our life-changing platforms, and we are in a fantastic position to execute on our strategy and continue the momentum we have built.
The last 10 years at AngioDynamics have been tremendously rewarding as we have transformed the company into a leading innovator of novel solutions that directly address the world's two leading causes of death. Within our med tech segment, we now have products addressing over a $10 billion global addressable market, and we have set ourselves up to be a physician partner and focus on expanding the applicability of these platforms to help more healthcare providers and their patients. With all of the work we have done, particularly over the last few years, the organization has earned enormous trust through the efficacy of our life-changing platforms, and we are in a fantastic position to execute on our strategy and continue the momentum we have built.
Speaker #3: Until my successor is appointed, I will continue to oversee the company’s strategic and financial initiatives and will continue with the company to ensure a seamless transition.
Speaker #3: I will have plenty of time to reflect before my transition occurs, but I wanted to take this opportunity to thank each and every one of our employees, our partners, and the talented healthcare professionals for the good work that I have had alongside during these last ten years.
Speaker #3: As we have collectively worked to help healthcare providers deliver the best care to patients with unmet needs, with that, we can open the line for questions.
Speaker #2: Thank you. We'll now be conducting a question and answer session. If you'd like to ask a question at this time, you may press star one from your telephone keypad, and a confirmation tone will indicate your line is in the question queue.
Operator: I worked with the board with regard to the timing of my retirement, and the board has established a search committee and is conducting a comprehensive process assisted by a leading executive search firm to identify our next CEO, which we expect to occur during fiscal 2027. Until my successor is appointed, I will continue to oversee the company's strategic and financial initiatives and will continue with the company to ensure a seamless transition. I will have plenty of time to reflect before my transition occurs, but I wanted to take this opportunity to thank each and every one of our employees, our partners, and the talented healthcare providers that I have had the good fortune to work alongside during these last 10 years as we have collectively worked to help healthcare providers deliver the best care to patients with unmet needs.
I worked with the board with regard to the timing of my retirement, and the board has established a search committee and is conducting a comprehensive process assisted by a leading executive search firm to identify our next CEO, which we expect to occur during fiscal 2027. Until my successor is appointed, I will continue to oversee the company's strategic and financial initiatives and will continue with the company to ensure a seamless transition. I will have plenty of time to reflect before my transition occurs, but I wanted to take this opportunity to thank each and every one of our employees, our partners, and the talented healthcare providers that I have had the good fortune to work alongside during these last 10 years as we have collectively worked to help healthcare providers deliver the best care to patients with unmet needs.
Speaker #2: You may like to press star two to ask a question if you'd like to join the queue. For participants using speaker equipment, it may be necessary to pick up your handset before pressing the star key. One moment, please.
Speaker #2: Poll for 'Will we' questions? Thank you. Our first question is from the line of Frank Takkinen with Lake Street Capital. Please proceed with your question.
Speaker #5: Great . Thank you for taking the questions , Jim . Congratulations on the retirement . Wishing you all the best in that new chapter hoping .
Speaker #5: Was to question with start at gross margin. It feels like that really outperformed nicely in the quarter, and obviously saw the guidance stay unchanged.
Speaker #5: I think I heard a comment around gross margin relatively staying stable, which would imply gross margin doing a little bit better than where consensus is at right now for the year.
Speaker #5: Any comments around gross margin expectations and why we shouldn't see that kind of mid-50% gross margin stay throughout the end of the year and into the following years?
Operator: With that, we can open the line for questions. Thank you. We'll now be conducting a question-and-answer session. If you'd like to ask a question at this time, you may press star one from your telephone keypad, and a confirmation tone to indicate your line is in the question queue. You may press star two if you'd like to withdraw your question from the queue. For participants using speaker equipment, it may be necessary to pick up your handset before pressing the star keys. One moment, please, while we pull for questions. Thank you. Our first question is from the line of Frank Takkinen with Lake Street Capital. Please proceed with your questions. Great. Thank you for taking the questions, Jim. Congratulations on the retirement. Wishing you all the best in that new chapter. I was hoping to start with a question around gross margin.
With that, we can open the line for questions.
Operator: Thank you. We'll now be conducting a question-and-answer session. If you'd like to ask a question at this time, you may press star one from your telephone keypad, and a confirmation tone to indicate your line is in the question queue. You may press star two if you'd like to withdraw your question from the queue. For participants using speaker equipment, it may be necessary to pick up your handset before pressing the star keys. One moment, please, while we pull for questions. Thank you. Our first question is from the line of Frank Takkinen with Lake Street Capital. Please proceed with your questions.
Speaker #4: Hi , Frank , Yeah . this is Steve . I'll take the gross margin question . So you're right . We were very pleased with the performance that we've seen on gross margin , particularly in the first half .
Speaker #4: And as we mentioned, there's a couple dynamics that are driving that. We're seeing positive price in both our MedTech and med device businesses.
Speaker #4: And we're seeing a benefit of the production related to us getting ready to do the move of some of those materials down to Costa Rica.
Speaker #4: Increased price, along with the mix shift to Med Tech and then some of those production volumes, are what we're seeing as a nice positive for gross margin in the first half.
Frank Takkinen: Great. Thank you for taking the questions, Jim. Congratulations on the retirement. Wishing you all the best in that new chapter. I was hoping to start with a question around gross margin.
Speaker #4: In the back half of the year , the price that we took is still going to continue to stay there . That mix shift will continue , but we're going to bit of a have a little under absorption as we move some of those final products out of Queensbury , and having them being produced by our third party manufacturing partner down in Costa Rica , you know , as we talked about this plan originally , we knew that there was going to be some of that structural under absorption .
Operator: It feels like that really outperformed nicely in the quarter and obviously saw the guidance stay unchanged. And I think I heard a comment around staying relatively stable, which would imply gross margin actually doing a little bit better than where the consensus is at right now for the year. Any comments around kind of gross margin expectations and why we shouldn't see that kind of mid-50% gross margin stay throughout the end of the year and into the following years? Yeah. Hi, Frank. This is Steve. I'll take the gross margin question. So you're right. We were very pleased with the performance that we've seen on gross margin, particularly in the first half. And as we mentioned, there's a couple of dynamics that are driving that.
It feels like that really outperformed nicely in the quarter and obviously saw the guidance stay unchanged. And I think I heard a comment around staying relatively stable, which would imply gross margin actually doing a little bit better than where the consensus is at right now for the year. Any comments around kind of gross margin expectations and why we shouldn't see that kind of mid-50% gross margin stay throughout the end of the year and into the following years?
Speaker #4: mentioned And we had that that would be somewhat offset by taking costs out . And that has been the overall plan , as we take some costs out of indirect labor .
Speaker #4: The good thing that our team has done is we've accelerated some of those costs coming out of the plant. So you're seeing that in the first half of the year.
Steve Trowbridge: Yeah. Hi, Frank. This is Steve. I'll take the gross margin question. So you're right. We were very pleased with the performance that we've seen on gross margin, particularly in the first half. And as we mentioned, there's a couple of dynamics that are driving that.
Speaker #4: So really , the dynamic going into the second half is some of those products . Now finalizing their move . According with our plans , you'll see some of that structural under absorption .
Operator: We're seeing positive price in both our med tech and our med device businesses, and we're seeing a benefit of the production related to us getting ready to do the move of some of those materials down to Costa Rica. So increased price, along with the mix shift to med tech, and then some of those production volumes are what we're seeing as a nice positive for gross margin in the first half. In the back half of the year, the price that we took is still going to continue to stay there, and that mix shift will continue, but we're going to have a little bit of a structural underabsorption as we move some of those final products out of Queensbury and having them being produced by our third-party manufacturing partner down in Costa Rica.
We're seeing positive price in both our med tech and our med device businesses, and we're seeing a benefit of the production related to us getting ready to do the move of some of those materials down to Costa Rica. So increased price, along with the mix shift to med tech, and then some of those production volumes are what we're seeing as a nice positive for gross margin in the first half. In the back half of the year, the price that we took is still going to continue to stay there, and that mix shift will continue, but we're going to have a little bit of a structural underabsorption as we move some of those final products out of Queensbury and having them being produced by our third-party manufacturing partner down in Costa Rica.
Speaker #4: You won't have the offsetting cost cuts . But that's because those costs have already come out . So that's really the dynamic and the between the first and the second half .
Speaker #5: Got it . Okay . That's helpful . And then maybe just my second for mechanical bit more talk a little about thrombectomy . I heard the comments around angiovac a more challenging year over year comp , but was curious if there's anything else going on in that business .
Speaker #5: We were hoping it would be a little bit stronger growth, but understand it was off a pretty tough comp. And then, maybe as a second part to that, if you could talk about kind of APEX return and some of the other work in right heart and what that might do to the growth profile of that line item over time.
Speaker #3: Yeah . Thanks for the question . Really , really pleased with the performance of Alpha VAC and PE as we're gaining new cases , new doctors and getting awarded kind of status in the hospital through VAC committees , getting , you know , quote unquote on the shelf in new accounts , the performance of inventory , in VAC is terrific .
Operator: As we talked about this plan originally, we knew that there was going to be some of that structural underabsorption, and we had mentioned that that would be somewhat offset by taking costs out. And that has been the overall plan as we take some costs out of indirect labor. The good thing that our team has done is we've accelerated some of those costs coming out of the plant. So you're seeing that in the first half of the year. So really, the dynamic going into the second half is some of those products now finalizing their move according with our plans. You'll see some of that structural underabsorption. You won't have the offsetting cost cuts, but that's because those costs have already come out. So that's really the dynamic and the difference between the first and the second half. Got it. Okay. That's helpful.
As we talked about this plan originally, we knew that there was going to be some of that structural underabsorption, and we had mentioned that that would be somewhat offset by taking costs out. And that has been the overall plan as we take some costs out of indirect labor. The good thing that our team has done is we've accelerated some of those costs coming out of the plant. So you're seeing that in the first half of the year. So really, the dynamic going into the second half is some of those products now finalizing their move according with our plans. You'll see some of that structural underabsorption. You won't have the offsetting cost cuts, but that's because those costs have already come out. So that's really the dynamic and the difference between the first and the second half.
Speaker #3: We see pictures every day, hear stories of new physicians using it because of the unique design elements that we innovatively put into the product.
Speaker #3: So, really excited about that. Continued growth at a strong level for a long time to come. AngioVac will be fine. If you look back a year ago, we had a really strong Q2, went down in revenue in Q3, and back up in Q4.
Speaker #3: There are cycles that just happen sometimes, so we're pleased. And you saw, I think we're up 11% in AngioVac in the first six months of the year.
Frank Takkinen: Got it. Okay. That's helpful.
Operator: And then maybe just for my second one, was hoping to talk a little bit more about mechanical thrombectomy. Heard the comments around AngioVac had a more challenging year-over-year comp, but was curious if there's anything else going on in that business. We were hoping it would be a little bit stronger growth, but understand it was off a pretty tough comp. And then maybe as a second part to that, if you could talk about kind of APEX-Return and some of the other work in right heart and what that might do to the growth profile of that line item over time. Yeah, Frank, thanks for the question. Really, really pleased with the performance of AlphaVac and PE as we're gaining new cases, new doctors, and getting awarded kind of status in the hospital through VAC committees, getting on the shelf in inventory in new accounts.
And then maybe just for my second one, was hoping to talk a little bit more about mechanical thrombectomy. Heard the comments around AngioVac had a more challenging year-over-year comp, but was curious if there's anything else going on in that business. We were hoping it would be a little bit stronger growth, but understand it was off a pretty tough comp. And then maybe as a second part to that, if you could talk about kind of APEX-Return and some of the other work in right heart and what that might do to the growth profile of that line item over time.
Speaker #3: we're really pleased with So the platform . It will be one of our key growth categories for a long time to come . We have two amazing products that work really well and that place , and it'll drive growth .
Speaker #3: And then, Steve, as far as—yeah.
Speaker #4: And then Frank , to follow up on the question on Alpha return , you know , as we've always said , we've got the best product on the market .
Speaker #4: We're very confident in that. We think when we take the AlphaVac product, we get that into the hands of physicians consistently.
Speaker #4: The we're getting feedback that is that it gives them what they need , and it's the best product that's out there . As we've talked about a hurdle to adoption in some areas because of of the way that the market has been conditioned has been the ability to then return the Blood Alpha back is designed upfront to limit blood loss and mitigate that .
Jim Clemmer: Yeah, Frank, thanks for the question. Really, really pleased with the performance of AlphaVac and PE as we're gaining new cases, new doctors, and getting awarded kind of status in the hospital through VAC committees, getting on the shelf in inventory in new accounts.
Speaker #4: But there's no doubt that the market is looking for an opportunity to return that blood in certain scenarios. And so we think that the Alpha Return product is really important for us to get over some of those initial humps, to have the past VAC if people choose, if they've been used to using competitive products.
Operator: The performance of AlphaVac is terrific. We see pictures every day, hear stories of new physicians using it because of the unique design elements that we innovatively put into the product. So really excited about that continued growth at a strong level for a long time to come. AngioVac will be fine. If you look back a year ago, we had a really strong Q2, and revenue went down in Q3 and back in Q4. There's cycles that just happen sometimes, so we're pleased. And you saw they grew up 11% in AngioVac in the first six months of the year. So we're really pleased with the platform. It will be one of our key growth categories for a long time to come. We have two amazing products that work really well in that place and will drive growth. And then Steve, as far as. Yeah.
The performance of AlphaVac is terrific. We see pictures every day, hear stories of new physicians using it because of the unique design elements that we innovatively put into the product. So really excited about that continued growth at a strong level for a long time to come. AngioVac will be fine. If you look back a year ago, we had a really strong Q2, and revenue went down in Q3 and back in Q4. There's cycles that just happen sometimes, so we're pleased. And you saw they grew up 11% in AngioVac in the first six months of the year. So we're really pleased with the platform. It will be one of our key growth categories for a long time to come. We have two amazing products that work really well in that place and will drive growth. And then Steve, as far as.
Speaker #4: We're really so excited about it. We've talked about the conversations we've been having with the FDA for a while. We were very pleased to get this over the finish line.
Speaker #4: We're excited about the IDE study , starting it and then getting this into the bag of our of our sales force , really as a way to take away an objection .
Speaker #4: And we expect it to be a catalyst to the accelerating growth in the future.
Speaker #5: Helpful. Thanks. Got it. Thanks for taking the questions.
Speaker #5: .
Speaker #4: Thank you . .
Speaker #4: Frank
Steve Trowbridge: Yeah.
Operator: And then, Frank, to follow up on the question on AlphaReturn, as we've always said, we've got the best product on the market. We're very confident in that. We think when we take the AlphaVac product, we get that into the hands of physicians. Consistently, the feedback that we're getting is that it gives them what they need, and it's the best product that's out there. As we've talked about, a hurdle to adoption in some areas because of the way that the market has been conditioned has been the ability to then return the blood. AlphaVac is designed upfront to limit blood loss and mitigate that, but there's no doubt that the market is looking for an opportunity to return that blood in certain scenarios.
And then, Frank, to follow up on the question on AlphaReturn, as we've always said, we've got the best product on the market. We're very confident in that. We think when we take the AlphaVac product, we get that into the hands of physicians. Consistently, the feedback that we're getting is that it gives them what they need, and it's the best product that's out there. As we've talked about, a hurdle to adoption in some areas because of the way that the market has been conditioned has been the ability to then return the blood. AlphaVac is designed upfront to limit blood loss and mitigate that, but there's no doubt that the market is looking for an opportunity to return that blood in certain scenarios.
Speaker #2: Thank you. The next questions are from the line of Bill Plavnik with Concord. Please proceed with your questions.
Speaker #6: Thanks . Great . Good morning and thanks for taking my questions . Just first , Jim know , I know You , congratulations ten years is a long time and it's you know , it's a lot of work that you've accomplished and some great outcomes .
Speaker #6: So, my hat's off to you, and you'll definitely be missed in terms of my questions. I want to start with prostate.
Speaker #6: I know you're only a few days in talk . Just change to the about the level one CPT code . How many insurers have really made that back end change to reflect the coding to change prevent the automatic denials ?
Operator: So we think that the AlphaReturn product is really important for us to get over some of those initial humps to have people choose AlphaVac if maybe in the past they've been used to using competitive products. So we're really excited about it. We've talked about the conversations we've been having with FDA for a while. We were very pleased to get this over the finish line. We're excited about the IDE study starting it, and then getting this into the bag of our sales force really as a way to take away an objection, and we expect it to be a catalyst to accelerating growth in the future. Got it. That's helpful. Thanks for taking the questions. Thank you, Frank. Thank you. The next questions are from the line of Bill Plovanic with Canaccord Genuity. Please proceed with your questions. Great. Thanks.
So we think that the AlphaReturn product is really important for us to get over some of those initial humps to have people choose AlphaVac if maybe in the past they've been used to using competitive products. So we're really excited about it. We've talked about the conversations we've been having with FDA for a while. We were very pleased to get this over the finish line. We're excited about the IDE study starting it, and then getting this into the bag of our sales force really as a way to take away an objection, and we expect it to be a catalyst to accelerating growth in the future.
Speaker #6: So far by your estimation ? And then I noticed capital strong really were was I mean that the saw , disposables a good .
Speaker #6: They were very strong. But it seems like capital was even stronger. And I'm curious, is buying that the case for prostate?
Speaker #6: is, you know, precursor to the systems to get ready to do procedures.
Frank Takkinen: Got it. That's helpful. Thanks for taking the questions.
Speaker #4: Bill , thanks for the question . Yeah . This is Hey , Steve and we want to congratulate Jim too . Although he's not going anywhere right away .
Steve Trowbridge: Thank you, Frank.
Operator: Thank you. The next questions are from the line of Bill Plovanic with Canaccord Genuity. Please proceed with your questions.
Speaker #4: So he's going to be with us for a while . So we're we're happy about that . And it'll be time to , to talk about everything that he's done .
Speaker #4: your On question on prostate , we're just a few days into it , so we don't have an estimate for changes that you were talking about , but it's for the something that our team is absolutely keyed in on .
Bill Plovanic: Great. Thanks.
Operator: Good morning, and thanks for taking my questions. Just first, Jim, congratulations. I know 10 years is a long time, and it's a lot of work that you've accomplished and some great outcomes. So hats off to you, and you'll definitely be missed. In terms of my questions, I want to start with prostate. I know you're only a few days in. Just talk about the change to the level one CPT code. How many insurers have really made that backend change to reflect the coding change to prevent the automatic denials so far by your estimation? And then I noticed that the capital was a really strong quarter. I mean, disposables were good. They saw a very strong, but it seems like capital was even stronger. And I'm curious, is that a precursor to the prostate as they're buying the systems to get ready to do procedures? Yeah.
Good morning, and thanks for taking my questions. Just first, Jim, congratulations. I know 10 years is a long time, and it's a lot of work that you've accomplished and some great outcomes. So hats off to you, and you'll definitely be missed. In terms of my questions, I want to start with prostate. I know you're only a few days in. Just talk about the change to the level one CPT code. How many insurers have really made that backend change to reflect the coding change to prevent the automatic denials so far by your estimation? And then I noticed that the capital was a really strong quarter. I mean, disposables were good. They saw a very strong, but it seems like capital was even stronger. And I'm curious, is that a precursor to the prostate as they're buying the systems to get ready to do procedures?
Speaker #4: We're going to continue to watch and monitor. We think that this is going to be a catalyst for us, particularly on the Medicare side.
Speaker #4: that's something that we're going to stay stay close So to . And watch . But we're pleased now with , you know , over the last year , we've been talking about the code going into effect .
Speaker #4: So, the turn of the calendar was a good move for us, and we're excited about that. On capital, there are two dynamics.
Speaker #4: Was strong. There was capital, also the capital sales that we talked about in the distribution channel move in France, that added some additional NanoKnife capital.
Speaker #4: But on top of that , we were still pretty pleased with the capital sales that we So as saw . we've mentioned , capital sales are mostly going to be in the international markets here in the US .
Speaker #4: It's going to be a lot of different mixture models to make sure that we get capital into the hands of our physicians. That could be through placement models, it could be through sales.
Speaker #4: I think the arbiter that we're looking at are those sales. And so we were really pleased with the nice increase in sales.
Steve Trowbridge: Yeah.
Operator: Hey, Bill. Thanks for the question. This is Steve. And we want to congratulate Jim, too, although he's not going anywhere right away. So he's going to be with us for a while. So we're happy about that, and we'll take time to talk about everything that he's done. On your question on prostate, we're just a few days into it, so we don't have an estimate for the changes that you were talking about, but it's something that our team is absolutely keyed in on, and we're going to continue to watch and monitor. We think that this is going to be a catalyst for us, particularly on the Medicare side. So it's something that we're going to stay close to and watch. But we're pleased. Now, over the last year, we've been talking about the code going into effect.
Hey, Bill. Thanks for the question. This is Steve. And we want to congratulate Jim, too, although he's not going anywhere right away. So he's going to be with us for a while. So we're happy about that, and we'll take time to talk about everything that he's done. On your question on prostate, we're just a few days into it, so we don't have an estimate for the changes that you were talking about, but it's something that our team is absolutely keyed in on, and we're going to continue to watch and monitor. We think that this is going to be a catalyst for us, particularly on the Medicare side. So it's something that we're going to stay close to and watch. But we're pleased. Now, over the last year, we've been talking about the code going into effect.
Speaker #4: And it's all coming from increased awareness and enthusiasm on the part of urologists. And it's really prostate that's driving the NanoKnife results that we've seen so far.
Speaker #7: And .
Speaker #6: Then just on EBITDA , you mentioned that , you know , the back half would be , I think , lower than the first half .
Speaker #6: And just directionally, how do we think of adjusted EBITDA in the third quarter? Is it going to be negative? And thanks for taking my questions.
Operator: So the turn of the calendar was a good move for us, and we're excited about that. On capital, there are two dynamics. Capital was strong. There was also the capital sales that we talked about in the distribution channel move in France that added some additional NanoKnife capital. But on top of that, we're still pretty pleased with the capital sales that we saw. So as we've mentioned, capital sales are mostly going to be in the international markets. Here in the US, it's going to be a mixture of different models to make sure that we get capital into the hands of our physicians. That could be through placement models. It could be through sales. I think the arbiter that we're looking at are those probe sales. And so we were really pleased with the nice increase in probe sales.
So the turn of the calendar was a good move for us, and we're excited about that. On capital, there are two dynamics. Capital was strong. There was also the capital sales that we talked about in the distribution channel move in France that added some additional NanoKnife capital. But on top of that, we're still pretty pleased with the capital sales that we saw. So as we've mentioned, capital sales are mostly going to be in the international markets. Here in the US, it's going to be a mixture of different models to make sure that we get capital into the hands of our physicians. That could be through placement models. It could be through sales. I think the arbiter that we're looking at are those probe sales. And so we were really pleased with the nice increase in probe sales.
Speaker #4: Yeah , thanks , Bill . So so on EBITDA , we just wanted to make sure , you know , we were very pleased with the performance that we've seen here in the first half in EBITDA .
Speaker #4: We think it does prove out that the model can generate positive EBITDA, can generate cash, as well as driving the top line.
Speaker #4: So excited to keep that also talked continuing. We've talked about wanting to balance that with investments that are necessary to continue to drive the top-line growth in those medtech businesses.
Speaker #4: And so we've talked about investments into feet on the street in terms of the sales force, as well as some of those R&D investments that Jim mentioned with his prepared remarks today for some of the nice trials that are coming up.
Speaker #4: So some of that's going to come into the back half. We don't expect negative in the third quarter, maybe just not as robust as what we saw in the first half.
Operator: It's all coming from increased awareness and enthusiasm on the part of urologists. It's really prostate that's driving the NanoKnife results that we've seen so far. Then just on EBITDA, you mentioned that the back half would be, I think, lower than the first half. Just directionally, how do we think of Adjusted EBITDA in Q3? Is it going to be negative? Thanks for taking my questions. Yeah. Thanks, Bill. On EBITDA, we just wanted to make sure we were very pleased with the performance that we've seen here in H1 in EBITDA. We think it does prove out that the model can generate positive EBITDA, can generate cash as well as driving the top line. We're excited to keep that continuing.
It's all coming from increased awareness and enthusiasm on the part of urologists. It's really prostate that's driving the NanoKnife results that we've seen so far.
Speaker #2: Thank you. The next question is in the line of Eduardo Martinez with H.C. Wainwright. Please see with your questions.
Bill Plovanic: Then just on EBITDA, you mentioned that the back half would be, I think, lower than the first half. Just directionally, how do we think of Adjusted EBITDA in Q3? Is it going to be negative? Thanks for taking my questions.
Speaker #7: Hi . This is Eduardo on for you . Congrats on the quarter . I had a few questions on Arion . You mentioned the CE mark , and I'm just curious what your expectations are for international sales .
Speaker #7: If there are any specific regions you guys are going to target, and if that would be associated with any increased sales spend.
Steve Trowbridge: Yeah. Thanks, Bill. On EBITDA, we just wanted to make sure we were very pleased with the performance that we've seen here in H1 in EBITDA. We think it does prove out that the model can generate positive EBITDA, can generate cash as well as driving the top line. We're excited to keep that continuing.
Speaker #7: And also quantify the opportunity and your expectations for this year.
Speaker #3: Thanks, Eduardo. Good question. We're really pleased with the fact that our team got the CE mark, and then our Orion commercial and clinical teams have really done a great job driving awareness outside of the US.
Operator: We've also talked about wanting to balance that with investments that are necessary to continue to drive the top line growth in those Med Tech businesses. So we've talked about investments into feet on the street in terms of the sales force, as well as some of those R&D investments that Jim mentioned with his prepared remarks today for some of the nice trials that are coming up. Some of that's going to come into the back half. We don't expect negative in Q3. Maybe just not as robust as what we saw in H1. Thank you. The next question is from the line of Eduardo Martinez with H.C. Wainwright. Please proceed with your questions. Hi. This is Eduardo for you. Congrats on the quarter. I had a few questions on Auryon.
We've also talked about wanting to balance that with investments that are necessary to continue to drive the top line growth in those Med Tech businesses. So we've talked about investments into feet on the street in terms of the sales force, as well as some of those R&D investments that Jim mentioned with his prepared remarks today for some of the nice trials that are coming up. Some of that's going to come into the back half. We don't expect negative in Q3. Maybe just not as robust as what we saw in H1.
Speaker #3: You know, atherectomy isn't chosen at the same rate in the US to treat PAD as it is here, but we've used a series of clinical forms and educational programs that our team has driven outside of the US to really give people confidence in Arion as a platform, the how, science. And it's important for us, works.
Speaker #3: Because once people see how the science works, how safe and effective the product is treating that artery in above or knee, it's below the flexible and safe.
Operator: Thank you. The next question is from the line of Eduardo Martinez with H.C. Wainwright. Please proceed with your questions.
Speaker #3: So it doesn't take a lot of hands-on user training by us, so we're able to use our really good distributor network to support growth and support customers during the use of the product.
Eduardo Martinez-Montes: Hi. This is Eduardo for you. Congrats on the quarter. I had a few questions on Auryon.
Speaker #3: So we've not identified or targeted yet a size of the market that we think we'll capture, but we're really pleased with the—the.
Operator: You mentioned the CE mark, and I'm just curious what your expectations are for international sales, if there are any specific regions you guys are going to target, and if that would be associated with any increased sales spend, and also if you could quantify the opportunity there and your expectations for this year. Thanks, Eduardo. A good question. We're really pleased with the fact that our team got the CE mark for Auryon, and then our commercial and clinical teams have really done a great job driving awareness outside of the US. Atherectomy isn't chosen at the same rate outside the US to treat PAD as it is here. But we've used a series of clinical forums, and educational programs that our team has driven outside of the US to really give people confidence in Auryon as a platform, how the science works.
You mentioned the CE mark, and I'm just curious what your expectations are for international sales, if there are any specific regions you guys are going to target, and if that would be associated with any increased sales spend, and also if you could quantify the opportunity there and your expectations for this year.
Speaker #3: Uptake already in people getting new . Our own systems , buying the disposables , treating patients with Pad and having really good you'll see our So over results .
Speaker #3: International sales creep up as this larger percentage of our overall Orien sales.
Jim Clemmer: Thanks, Eduardo. A good question. We're really pleased with the fact that our team got the CE mark for Auryon, and then our commercial and clinical teams have really done a great job driving awareness outside of the US. Atherectomy isn't chosen at the same rate outside the US to treat PAD as it is here. But we've used a series of clinical forums, and educational programs that our team has driven outside of the US to really give people confidence in Auryon as a platform, how the science works.
Speaker #7: really helpful . And also Got it . That's on Orion , you mentioned expansion into coronary coronary applications . I'm just curious if you had a timeline for that .
Speaker #7: Also, any increased spend, if that's something we can expect in the R&D line item this year, in 2026.
Speaker #4: I wouldn't expect a significant amount of spend in the R&D line item this year. We talk as about coronary. Clearly, it's a strategic imperative of ours to take the product and move into the coronary space.
Speaker #4: It's a little bit of a longer term initiative . As we talked about , it's probably a PMA trial . So , you know , we gave some highlights in the past of the ability to take our current platform technologies and through clinical and regulatory pathway expansion , move into additional Tams .
Operator: It's important for us because once people see how the science works, how safe and effective the product is in treating that artery, above or below the knee, flexible and safe, so it doesn't take a lot of hands-on user training by us. We're able to use our really good distributor network to support growth, support customers during the use of the product. We've not identified or targeted yet a size of the market that we think will capture, but we're really pleased with the uptake already in people getting new Auryon systems, buying the disposables, treating patients with PAD, and having really good results. Over time, you'll see our international sales creep up as a larger percentage of our overall Auryon sales. Got it. That's really helpful. Also on Auryon, you mentioned expansion into coronary applications.
It's important for us because once people see how the science works, how safe and effective the product is in treating that artery, above or below the knee, flexible and safe, so it doesn't take a lot of hands-on user training by us. We're able to use our really good distributor network to support growth, support customers during the use of the product. We've not identified or targeted yet a size of the market that we think will capture, but we're really pleased with the uptake already in people getting new Auryon systems, buying the disposables, treating patients with PAD, and having really good results. Over time, you'll see our international sales creep up as a larger percentage of our overall Auryon sales.
Speaker #4: A very good example of that is Orion moving into the coronary space. But it's not something that's going to be impactful in terms of, in this, the spend year.
Speaker #7: Got it. Thanks so much for taking the questions, and congrats again on the quarter.
Speaker #8: you Thank .
Speaker #2: Thank you. At this time, I'll hand the call back to Mr. James Clemmer for closing remarks.
Speaker #3: Thanks, Rob. Rob, I'd like to thank all of our employees here at AngioDynamics who've made these great results possible by their commitment and dedication to our customers and our products.
Eduardo Martinez-Montes: Got it. That's really helpful. Also on Auryon, you mentioned expansion into coronary applications.
Speaker #3: So, we've changed this company by its portfolio. You've seen us become active portfolio managers to make sure our company's positioned in the right places, at the right time, with the right products for future growth.
Operator: I'm just curious if you had a timeline for that and also any increased spend, if that's something we can expect in the R&D line item this year in 2026. I wouldn't expect a significant amount of spend in the R&D line item this year as we talk about coronary. Clearly, it's a strategic imperative of ours to take the product and move into the coronary space. It's a little bit of a longer-term initiative, as we talked about. It's probably a PMA trial. So we gave some highlights in the past of the ability to take our current platform technologies and through clinical and regulatory pathway expansion, move into additional hands. A very good example of that is Auryon moving into the coronary space, but it's not something that's going to be impactful in terms of the spend in this year. Got it.
I'm just curious if you had a timeline for that and also any increased spend, if that's something we can expect in the R&D line item this year in 2026.
Speaker #3: The company is doing a really good job executing today, but we're also building for tomorrow and investing in opportunities to expand the application of our products geographically.
Jim Clemmer: I wouldn't expect a significant amount of spend in the R&D line item this year as we talk about coronary. Clearly, it's a strategic imperative of ours to take the product and move into the coronary space. It's a little bit of a longer-term initiative, as we talked about. It's probably a PMA trial. So we gave some highlights in the past of the ability to take our current platform technologies and through clinical and regulatory pathway expansion, move into additional hands. A very good example of that is Auryon moving into the coronary space, but it's not something that's going to be impactful in terms of the spend in this year.
Speaker #3: A new and clinical applications. So we're really pleased with where the company is headed. We can't wait to share more results with you in the future. Thanks to all of our supporters.
Speaker #3: teammates .
Speaker #2: This will conclude today's conference. You may disconnect your lines at this time. Thank you for your participation. Have a wonderful day.
Eduardo Martinez-Montes: Got it.
Operator: Thanks so much for taking the questions, and congrats again on the quarter. Thank you. Thank you. At this time, I'll hand the call back to Mr. Jim Clemmer for closing remarks. Thanks, Rob. Rob, I'd like to thank all of our employees here at AngioDynamics who've made these great results possible by their commitment and dedication to our customer and our products. So we've changed this company by its portfolio. You've seen us become active portfolio managers to make sure our company's positioned in the right places at the right time with the right products for future growth. The company's doing a really good job executing today, but we're also building for tomorrow and investing in opportunities to expand the application of our products geographically, and in new clinical applications. So we're really pleased with where the company's headed.
Thanks so much for taking the questions, and congrats again on the quarter. Thank you.
Operator: Thank you. At this time, I'll hand the call back to Mr. Jim
Jim Clemmer: Clemmer for closing remarks. Thanks, Rob. Rob, I'd like to thank all of our employees here at AngioDynamics who've made these great results possible by their commitment and dedication to our customer and our products. So we've changed this company by its portfolio. You've seen us become active portfolio managers to make sure our company's positioned in the right places at the right time with the right products for future growth. The company's doing a really good job executing today, but we're also building for tomorrow and investing in opportunities to expand the application of our products geographically, and in new clinical applications. So we're really pleased with where the company's headed.
Operator: We can't wait to share more results with you in the future. Thanks to all of our teammates. This will conclude today's conference. You may disconnect your lines at this time. Thank you for your participation. Have a wonderful day.
We can't wait to share more results with you in the future. Thanks to all of our teammates.
Operator: This will conclude today's conference. You may disconnect your lines at this time. Thank you for your participation. Have a wonderful day.