UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549



FORM 8-K

CURRENT REPORT
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934

Date of Report (Date of earliest event reported):  October 2, 2025

AngioDynamics, Inc.
(Exact Name of Registrant as Specified in Charter)

Delaware
000-50761
11-3146460
     
(State or Other Jurisdiction of Incorporation)
(Commission File Number)
(IRS Employer Identification No.)

14 Plaza Drive, Latham, New York

12110
     
(Address of Principal Executive Offices)

(Zip Code)

(518) 795-1400

(Registrant’s telephone number, including area code)
 
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:


Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
 

Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
 

Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2 (b))
 

Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4 (c))
 
Securities registered pursuant to Section 12(b) of the Act:
 
Title of each class
Trading Symbol(s)

Name of each exchange on which
registered
       
Common Stock, par value $0.01 per share
ANGO

NASDAQ Global Select Market
 
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
 
Emerging growth company
 
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
 


Item 2.02 – Results of Operations and Financial Condition.
 

On October 2, 2025, AngioDynamics, Inc. (“AngioDynamics”) issued a press release announcing financial results for the fiscal first quarter ended August 31, 2025. A copy of the press release is furnished herewith as Exhibit 99.1.

The information set forth in Item 2.02 of this Form 8-K (including Exhibit 99.1) shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities under that Section. Furthermore, such information shall not be deemed to be incorporated by reference into any filing under the Securities Act of 1933, as amended (the “Securities Act”), or the Exchange Act, except as shall be expressly set forth by specific reference in such a filing.

Item 7.01 – Regulation FD Disclosure.

Presentation slides discussing AngioDynamics and its fiscal first quarter ended August 31, 2025 are furnished herewith as Exhibit 99.2.

The presentation slides furnished pursuant to Item 7.01 of this Form 8-K (including Exhibit 99.2) shall not be deemed “filed” for purposes of Section 18 of the Exchange Act, or otherwise subject to the liabilities under that Section. Furthermore, the presentation slides shall not be deemed to be incorporated by reference into any filing under the Securities Act or the Exchange Act.

Forward-Looking Statements

This document and its attachments contain forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements regarding AngioDynamics’ expected future financial position, results of operations, cash flows, business strategy, budgets, projected costs, capital expenditures, products, competitive positions, growth opportunities, plans and objectives of management for future operations, as well as statements that include the words such as “expects,” “reaffirms,” “intends,” “anticipates,” “plans,” “believes,” “seeks,” “estimates,” “projects”, “optimistic,” or variations of such words and similar expressions, are forward-looking statements. These forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties. Investors are cautioned that actual events or results may differ materially from AngioDynamics’ expectations, expressed or implied. Factors that may affect the actual results achieved by AngioDynamics include, without limitation, the scale and scope of the COVID-19 global pandemic, the ability of AngioDynamics to develop its existing and new products, technological advances and patents attained by competitors, infringement of AngioDynamics’ technology or assertions that AngioDynamics’ technology infringes the technology of third parties, the ability of AngioDynamics to effectively compete against competitors that have substantially greater resources, future actions by the FDA or other regulatory agencies, domestic and foreign health care reforms and government regulations, results of pending or future clinical trials, overall economic conditions (including inflation, tariffs, labor shortages and supply chain challenges including the cost and availability of raw materials), the results of on-going litigation, challenges with respect to third-party distributors or joint venture partners or collaborators, the results of sales efforts, the effects of product recalls and product liability claims, changes in key personnel, the ability of AngioDynamics to execute on strategic initiatives, the effects of economic, credit and capital market conditions, general market conditions, market acceptance, foreign currency exchange rate fluctuations, the effects on pricing from group purchasing organizations and competition, the ability of AngioDynamics to obtain regulatory clearances or approval of its products, or to integrate acquired businesses, as well as the risk factors listed from time to time in AngioDynamics’ SEC filings, including but not limited to its Annual Report on Form 10-K for the year ended May 31, 2025. AngioDynamics does not assume any obligation to publicly update or revise any forward-looking statements for any reason.


Item 9.01 – Financial Statements and Exhibits.

(d)
Exhibits.

Exhibit No.
Description
   
Press Release, dated October 2, 2025.
   
Presentation, dated October 2, 2025.


SIGNATURE

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 
ANGIODYNAMICS, INC.
 
(Registrant)
     
Date:  October 2, 2025
By: /s/ Lawrence T. Weiss
 
Name:
Lawrence T. Weiss
 
Title:
Senior Vice President, Chief Legal Officer and Corporate Secretary




Exhibit 99.1

AngioDynamics Reports Fiscal Year 2026 First Quarter Financial Results; Med Tech Growth of 26.1% Drives Continued Momentum


Med Tech segment delivers fourth consecutive quarter of over 20% revenue growth

Reported Adjusted EBITDA of $2.2 million compared to ($0.2) million in the prior year

Continues to expect to be cash flow positive for the full fiscal year 2026

Raised full year FY 2026 guidance for net sales, Med Tech net sales growth, Adjusted EBITDA and Adjusted EPS

LATHAM, N.Y.--(BUSINESS WIRE)— Oct. 2, 2025-- AngioDynamics, Inc. (NASDAQ: ANGO), a leading and transformative medical technology company focused on restoring healthy blood flow in the body’s vascular system, expanding cancer treatment options, and improving quality of life for patients, today announced financial results for the first quarter of fiscal year 2026, which ended August 31, 2025.

Fiscal Year 2026 First Quarter Highlights


Quarter Ended
August 31, 2025
Pro Forma* YoY Growth
Net Sales
$75.7 million
12.2%
Med Tech Net Sales
$35.3 million
26.1%
Med Device Net Sales
$40.4 million
2.3%


GAAP gross margin of 55.3%

GAAP loss per share of $0.26

Adjusted loss per share of $0.10

Adjusted EBITDA of $2.2 million

Ended fiscal 2026 first quarter with $38.8 million in cash and cash equivalents, ahead of expectations, continues to expect to be cash flow positive for the full year FY 2026

First patients enrolled in both the AMBITION BTK and RECOVER-AV trials

NanoKnife PRESERVE study published in the journal of European Urology

*Pro forma results exclude the Dialysis and BioSentry businesses divested in June 2023 and the PICC,  Midline and tip location product portfolios divested in February 2024, as well as the discontinued Radiofrequency and Syntrax support catheter products in February 2024.

"We had an outstanding first quarter as we continued to build off of the strong momentum created in fiscal 2025," commented Jim Clemmer, President and Chief Executive Officer of AngioDynamics, Inc. "Our strategy to bring unique platform technologies to large, fast growing global markets has paid off as we reported our fourth quarter in a row of MedTech growth of over 20%. This continued performance, combined with our disciplined focus on operational excellence, is driving sustained profitable growth.”

1

Mr. Clemmer continued, “Our exceptional team is executing our vision to deliver transformative technologies that expand treatment options and help patients live healthier, happier lives. With our superior technologies supported by our clinical investments and the strength of our balance sheet, we remain well-positioned to drive consistent, profitable growth, and deliver sustained value creation during the balance of 2026 and beyond.”

Fiscal Year 2026 First Quarter Financial Results

Unless otherwise noted, all financial comparisons below are presented on a pro forma basis excluding the Dialysis and BioSentry businesses divested in June 2023, the PICC, Midline, and tip location product portfolios divested in February 2024, and the RadioFrequency and Syntrax support catheter products discontinued in February 2024.

Net sales for the first quarter of fiscal year 2026 were $75.7 million, an increase of 12.2% compared to the prior-year quarter.

Med Tech net sales were $35.3 million, a 26.1% increase from $28.0 million in the prior-year period. Med Tech includes the Auryon peripheral atherectomy platform, the thrombus management platform and the NanoKnife irreversible electroporation platform.

Growth during the quarter was driven by solid performance across the Med Tech segment. Auryon sales were $16.5 million an increase of 20.1%, our Mechanical Thrombectomy business, which includes AngioVac and AlphaVac, delivered sales of $11.3 million, an increase of 41.2%, and NanoKnife sales were $6.4 million, an increase of 26.7%, including 31.3% growth in probes.

Med Device net sales were $40.4 million, a 2.3% increase compared to $39.5 million in the prior-year period.

Gross margin for the first quarter of fiscal 2026 was 55.3%, which was 90 basis points higher compared to the first quarter of fiscal 2025, and 260 basis points higher sequentially from 52.7% in the fourth quarter of fiscal 2025, primarily due to increased  Med Tech revenue, as well as operational efficiencies.  Gross margin included $1.7 million of tariff expense.

The Company recorded a GAAP net loss of $10.9 million, or a loss per share of $0.26, in the first quarter of fiscal 2026. Excluding the items shown in the non-GAAP reconciliation table below, adjusted net loss for the first quarter of fiscal 2026 was $4.2 million, or a loss per share of $0.10. This compares to an adjusted net loss during the fiscal first quarter of 2025 of $4.4 million, or a loss per share of $0.11.

2

Adjusted EBITDA in the first quarter of fiscal 2026, excluding the items shown in the non-GAAP reconciliation table below, was $2.2 million, compared to $(0.2) million in the first quarter of fiscal 2025.

In the first quarter of fiscal 2026, the Company used $17.1 million of cash.  The Company’s first fiscal quarter has historically exhibited the highest utilization of cash during the year, and the first quarter of fiscal 2026 was better than the Company’s expectations, resulting in the use of less cash than expected. The Company continues to expect to be cash flow positive for the full year fiscal 2026.

At August 31, 2025, the Company had $38.8 million in cash and cash equivalents compared to $55.9 million in cash and cash equivalents at May 31, 2025. The Company maintains a debt-free balance sheet.

First Patient Enrolled in AMBITION BTK Trial

During the quarter, the Company announced that it achieved a significant clinical milestone with the enrollment of the first patient in the AMBITION BTK trial, a prospective, multicenter, randomized controlled trial designed to investigate the clinical safety and effectiveness of the Auryon Atherectomy System in treating challenging below-the-knee lesions in patients with Critical Limb Ischemia. The trial will include up to 224 patients at up to 30 sites, with a companion registry enrolling up to 1,500 additional patients, representing the Company's continued commitment to advancing clinical evidence for the treatment of peripheral artery disease and expanding the clinical applications for the Auryon platform.

First Patient Enrolled in RECOVER-AV Clinical Trial

During the quarter, the Company announced the first patient enrollment in the RECOVER-AV clinical trial, a prospective, multi-center, multi-national, single-arm study evaluating the AlphaVac F1885 System for the treatment of acute, intermediate-risk pulmonary embolism. The study builds on the existing U.S. FDA 510(k) clearance and European CE Mark approval to assess mechanical thrombectomy treatment and long-term functional outcomes in intermediate-risk PE patients across Europe, Canada, and Hong Kong. The trial will enroll patients at up to 20 hospital-based sites and follows patients for 12 months, with functional and quality-of-life outcomes assessed at 30 days and 12 months, representing the Company's continued commitment to expanding its global clinical presence and generating evidence-based data to support broader access to life-saving PE treatment.

3

NanoKnife PRESERVE Study Results Published in Leading European Journal

During the quarter, the Company announced the publication of results from the PRESERVE study in European Urology, a leading journal in urologic research. The study assessed the safety and effectiveness of irreversible electroporation with the NanoKnife System to ablate prostate tissue in patients with intermediate-risk prostate cancer. The PRESERVE clinical study met its primary effectiveness endpoint, with 84.0% of men free from in-field, clinically significant disease at 12 months post-procedure. The study also demonstrated strong quality-of-life outcomes, with urinary continence largely preserved (97% at baseline vs. 96% at 12 months) and 84% of patients with good baseline sexual function at 12 months, reinforcing the NanoKnife System's role in providing effective treatment while preserving quality of life.

Fiscal Year 2026 Financial Guidance

For fiscal year 2026 the company now expects:

Guidance Metric
Guidance Action
Current Guidance
(as of October 2, 2025)
Previous Guidance
(as of July 15, 2025)
Net Sales
Increased
$308 - $313 million
$305 - $310 million
       
Med Tech Net Sales Growth
Increased
14% - 16%
12% - 15%
       
Med Device Net Sales Growth
Unchanged
Flat
Flat
       
Gross Margin
Unchanged
53.5% - 55.5%
53.5% - 55.5%
       
Adjusted EBITDA
Increased
$6.0 - $10.0 million
$3.0 - $8.0 million
       
Adjusted EPS
Increased
($0.33) – ($0.23)
($0.35) – ($0.25)
       
Free Cash Flow
Unchanged
Positive for full year FY 2026
Positive for full year FY 2026

Tariff Related Guidance Assumptions

For the full fiscal year 2026, the company continues to expect a $4.0 - $6.0 million impact from tariffs, which are included in the above provided guidance.

All assumptions made related to expected tariff impacts are based on the Company’s point of view on the current tariff situation, as of October 2, 2025. As the situation is fluid, these assumptions may change in the future.

Conference Call

The Company’s management will host a conference call at 8:00 a.m. ET the same day to discuss the results. To participate in the conference call, dial 1-877-407-0784 (domestic) or +1-201-689-8560 (international). This conference call will also be webcast and can be accessed from the “Investors” section of the AngioDynamics website at www.angiodynamics.com. The webcast replay of the call will be available at the same site approximately one hour after the end of the call.

A recording of the call will also be available, until Thursday, October 09, 2025 at 11:59 PM ET. To hear this recording, dial 1-844-512-2921 (domestic) or +1-412-317-6671 (international) and enter the passcode 13755707.

4

Use of Non-GAAP Measures

Management uses non-GAAP measures to establish operational goals and believes that non-GAAP measures may assist investors in analyzing the underlying trends in AngioDynamics' business over time. Investors should consider these non-GAAP measures in addition to, not as a substitute for or as superior to, financial reporting measures prepared in accordance with GAAP. In this news release, AngioDynamics has reported pro forma results, adjusted EBITDA, adjusted net income and adjusted earnings per share. Management uses these measures in its internal analysis and review of operational performance. Management believes that these measures provide investors with useful information in comparing AngioDynamics' performance over different periods. By using these non-GAAP measures, management believes that investors get a better picture of the performance of AngioDynamics' underlying business. Management encourages investors to review AngioDynamics' financial results prepared in accordance with GAAP to understand AngioDynamics' performance taking into account all relevant factors, including those that may only occur from time to time but have a material impact on AngioDynamics' financial results. Please see the tables that follow for a reconciliation of non-GAAP measures to measures prepared in accordance with GAAP.

About AngioDynamics, Inc.

AngioDynamics is a leading and transformative medical technology company focused on restoring healthy blood flow in the body’s vascular system, expanding cancer treatment options and improving quality of life for patients.

The Company’s innovative technologies and devices are chosen by talented physicians in fast-growing healthcare markets to treat unmet patient needs. For more information, visit www.angiodynamics.com.

5

Safe Harbor

This release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements regarding AngioDynamics' expected future financial position, results of operations, cash flows, business strategy, budgets, projected costs, capital expenditures, products, competitive positions, growth opportunities, plans and objectives of management for future operations, as well as statements that include the words such as "expects," "reaffirms," "intends," "anticipates," "plans," "believes," "seeks," "estimates," "projects," "optimistic," or variations of such words and similar expressions, are forward-looking statements. These forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties. Investors are cautioned that actual events or results may differ materially from AngioDynamics' expectations, expressed or implied. Factors that may affect the actual results achieved by AngioDynamics include, without limitation, the scale and scope of the COVID-19 global pandemic, the ability of AngioDynamics to develop its existing and new products, technological advances and patents attained by competitors, infringement of AngioDynamics' technology or assertions that AngioDynamics' technology infringes the technology of third parties, the ability of AngioDynamics to effectively compete against competitors that have substantially greater resources, future actions by the FDA or other regulatory agencies, domestic and foreign health care reforms and government regulations, results of pending or future clinical trials, overall economic conditions (including inflation, tariffs, labor shortages and supply chain challenges including the cost and availability of raw materials), the results of on-going litigation, challenges with respect to third-party distributors or joint venture partners or collaborators, the results of sales efforts, the effects of product recalls and product liability claims, changes in key personnel, the ability of AngioDynamics to execute on strategic initiatives, the effects of economic, credit and capital market conditions, general market conditions, market acceptance, foreign currency exchange rate fluctuations, the effects on pricing from group purchasing organizations and competition, the ability of AngioDynamics to obtain regulatory clearances or approval of its products, or to integrate acquired businesses, as well as the risk factors listed from time to time in AngioDynamics' SEC filings, including but not limited to its Annual Report on Form 10-K for the year ended May 31, 2025. AngioDynamics does not assume any obligation to publicly update or revise any forward-looking statements for any reason.

Investors:
Stephen Trowbridge
Executive Vice President & CFO
518-795-1408
strowbridge@angiodynamics.com

Media:
Saleem Cheeks
Vice President, Communications
518-795-1174
scheeks@angiodynamics.com

6

ANGIODYNAMICS, INC. AND SUBSIDIARIES
CONSOLIDATED INCOME STATEMENTS
(in thousands, except per share data)

   
Three Months Ended
 
         
As Reported (1)
   
Pro Forma
Adjustments (2)
   
Pro Forma
 
   
Aug 31, 2025
   
Aug 31, 2024
   
Aug 31, 2024
   
Aug 31, 2024
 
               
(unaudited)
       
                         
Net sales
 
$
75,711
   
$
67,491
     
9
   
$
67,500
 
Cost of sales (exclusive of intangible amortization)
   
33,854
     
30,767
     
(2
)
   
30,765
 
Gross margin
   
41,857
     
36,724
     
11
     
36,735
 
% of net sales
   
55.3
%
   
54.4
%
           
54.4
%
                                 
Operating expenses
                               
Research and development
   
6,417
     
6,285
     
     
6,285
 
Sales and marketing
   
28,130
     
25,605
     
     
25,605
 
General and administrative
   
12,555
     
10,975
     
     
10,975
 
Amortization of intangibles
   
2,653
     
2,570
     
     
2,570
 
Change in fair value of contingent consideration
   
     
76
     
     
76
 
Acquisition, restructuring and other items, net
   
2,758
     
4,311
     
154
     
4,465
 
Total operating expenses
   
52,513
     
49,822
     
154
     
49,976
 
Operating loss
   
(10,656
)
   
(13,098
)
   
(143
)
   
(13,241
)
Interest income (expense), net
   
(4
)
   
606
     
     
606
 
Other expense, net
   
(178
)
   
(173
)
   
     
(173
)
Total other income (expense), net
   
(182
)
   
433
     
     
433
 
Loss before income tax benefit
   
(10,838
)
   
(12,665
)
   
(143
)
   
(12,808
)
Income tax expense
   
65
     
133
     
     
133
 
Net loss
 
$
(10,903
)
 
$
(12,798
)
 
$
(143
)
 
$
(12,941
)
                                 
Loss per share
                               
Basic
 
$
(0.26
)
 
$
(0.31
)
         
$
(0.32
)
Diluted
 
$
(0.26
)
 
$
(0.31
)
         
$
(0.32
)
                                 
Weighted average shares outstanding
                               
Basic
   
41,174
     
40,653
             
40,653
 
Diluted
   
41,174
     
40,653
             
40,653
 

(1)  Reflects the Company's US GAAP consolidated financial statements before pro forma adjustments related to the sale of the Dialysis and BioSentry Businesses on June 8, 2023, the sale of the PICCs and Midlines Businesses on February 15, 2024 and the discontinuation of the RadioFrequency Ablation and Syntrax products ("the Businesses") as of February 29, 2024, for the three months ended August 31, 2024.

(2) Reflects the elimination of revenues and expenses representing the operating results from the sales and discontinuation of the Businesses.

7

ANGIODYNAMICS, INC. AND SUBSIDIARIES
GAAP TO NON-GAAP RECONCILIATION
(in thousands, except per share data)

Reconciliation of Net Loss to non-GAAP Adjusted Net Loss and Pro Forma Adjusted Net Loss:

   
Three Months Ended
 
         
As Reported (1)
   
Pro Forma
Adjustments (2)
   
Pro Forma
 
   
Aug 31, 2025
   
Aug 31, 2024
   
Aug 31, 2024
   
Aug 31, 2024
 
   
(unaudited)
 
                         
Net loss
 
$
(10,903
)
 
$
(12,798
)
 
$
(143
)
 
$
(12,941
)
                                 
Amortization of intangibles
   
2,653
     
2,570
     
     
2,570
 
Change in fair value of contingent consideration
   
     
76
     
     
76
 
Acquisition, restructuring and other items, net (3)
   
2,758
     
4,311
     
154
     
4,465
 
Tax effect of non-GAAP items (4)
   
1,313
     
1,446
     
(3
)
   
1,443
 
Adjusted net loss
 
$
(4,179
)
 
$
(4,395
)
 
$
8
   
$
(4,387
)

Reconciliation of Diluted Loss and Pro Forma Diluted Loss Per Share to non-GAAP Adjusted and Pro Forma Adjusted Diluted Loss Per Share:

   
Three Months Ended
 
         
As Reported (1)
   
Pro Forma
Adjustments (2)
   
Pro Forma
 
   
Aug 31, 2025
   
Aug 31, 2024
   
Aug 31, 2024
   
Aug 31, 2024
 
   
(unaudited)
             
                         
Diluted loss per share
 
$
(0.26
)
 
$
(0.31
)
 
$
(0.01
)
 
$
(0.32
)
                                 
Amortization of intangibles
   
0.06
     
0.06
     
0.00
     
0.06
 
Change in fair value of contingent consideration
   
0.00
     
0.00
     
0.00
     
0.00
 
Acquisition, restructuring and other items, net (3)
   
0.07
     
0.10
     
0.00
     
0.10
 
Tax effect of non-GAAP items (4)
   
0.03
     
0.04
     
0.00
     
0.04
 
Adjusted diluted loss per share
 
$
(0.10
)
 
$
(0.11
)
 
$
0.00
   
$
(0.11
)
                                 
Adjusted diluted sharecount (5)
   
41,174
     
40,653
     
40,653
     
40,653
 

(1)  Reflects the Company's US GAAP consolidated financial statements before pro forma adjustments related to the sale of the Dialysis and BioSentry Businesses on June 8, 2023, the sale of the PICCs and Midlines Businesses on February 15, 2024 and the discontinuation of the RadioFrequency Ablation and Syntrax products ("the Businesses") as of February 29, 2024, for the three months ended August 31, 2024.
(2) Reflects the elimination of revenues and expenses representing the operating results from the sales and discontinuation of the Businesses.
(3)  Includes costs related to merger and acquisition activities, restructuring, and unusual items, including asset impairments and write-offs, certain litigation, and other items.
(4) Adjustment to reflect the income tax provision on a non-GAAP basis has been calculated assuming no valuation allowance on the Company's U.S. deferred tax assets and an effective tax rate of 23% for the periods ended August 31, 2025 and 2024.
(5) Diluted shares may differ for non-GAAP measures as compared to GAAP due to a GAAP loss.

8

ANGIODYNAMICS, INC. AND SUBSIDIARIES
GAAP TO NON-GAAP RECONCILIATION (Continued)
(in thousands, except per share data)

Reconciliation of Net Loss and Pro Forma Net Loss to Adjusted EBITDA and Pro Forma Adjusted EBITDA:

   
Three Months Ended
 
         
As Reported (1)
   
Pro Forma
Adjustments (2)
   
Pro Forma
 
   
Aug 31, 2025
   
Aug 31, 2024
   
Aug 31, 2024
   
Aug 31, 2024
 
   
(unaudited)
             
                         
Net loss
 
$
(10,903
)
 
$
(12,798
)
 
$
(143
)
 
$
(12,941
)
                                 
Income tax expense
   
65
     
133
     
     
133
 
Interest expense (income), net
   
4
     
(606
)
   
     
(606
)
Depreciation and amortization
   
5,950
     
6,785
     
     
6,785
 
Change in fair value of contingent consideration
   
     
76
     
     
76
 
Stock based compensation
   
4,470
     
3,205
     
     
3,205
 
Acquisition, restructuring and other items, net (3)
   
2,574
     
3,042
     
154
     
3,196
 
Adjusted EBITDA
 
$
2,160
   
$
(163
)
 
$
11
   
$
(152
)

(1)  Reflects the Company's US GAAP consolidated financial statements before pro forma adjustments related to the sale of the Dialysis and BioSentry Businesses on June 8, 2023, the sale of the PICCs and Midlines Businesses on February 15, 2024 and the discontinuation of the RadioFrequency Ablation and Syntrax products ("the Businesses") as of February 29, 2024, for the three months ended August 31, 2024.
(2) Reflects the elimination of revenues and expenses representing the operating results from the sales and discontinuation of the Businesses.
(3)  Includes costs related to merger and acquisition activities, restructuring, and unusual items, including asset impairments and write-offs, certain litigation, and other items.

9

ANGIODYNAMICS, INC. AND SUBSIDIARIES
ACQUISITION, RESTRUCTURING, AND OTHER ITEMS, NET DETAIL
(in thousands)

   
Three Months Ended
 
(in thousands)
 
Aug 31, 2025
   
Aug 31, 2024
 
Legal (1)
 
$
213
   
$
507
 
Plant closure (2)
   
2,345
     
3,589
 
Transition service agreement (3)
   
(302
)
   
(507
)
Other
   
502
     
722
 
Total
 
$
2,758
   
$
4,311
 

(1)
Legal expenses related to litigation that is outside the normal course of business.

(2)
Plant closure expense, related to the restructuring of our manufacturing footprint which was announced on January 5, 2024.

(3)
Transition services agreements that were entered into with Merit and Spectrum.

10

ANGIODYNAMICS, INC. AND SUBSIDIARIES
NET SALES BY PRODUCT CATEGORY AND BY GEOGRAPHY
(in thousands)

   
Three Months Ended
             
         
As Reported (1)
   
Pro Forma
Adjustments (2)
   
Pro Forma
   
Actual
   
Pro Forma
 
   
Aug 31, 2025
   
Aug 31, 2024
   
Aug 31, 2024
   
Aug 31, 2024
   
% Growth
   
% Growth
 
               
(unaudited)
                   
Net Sales
                                   
Med Tech
 
$
35,261
   
$
27,969
   
$
   
$
27,969
     
26.1
%
   
26.1
%
Med Device
   
40,450
     
39,522
     
9
     
39,531
     
2.3
%
   
2.3
%
   
$
75,711
   
$
67,491
   
$
9
   
$
67,500
     
12.2
%
   
12.2
%
                                                 
Net Sales
                                               
United States
 
$
66,456
   
$
59,481
   
$
10
   
$
59,491
     
11.7
%
   
11.7
%
International
   
9,255
     
8,010
     
(1
)
   
8,009
     
15.5
%
   
15.6
%
   
$
75,711
   
$
67,491
   
$
9
   
$
67,500
     
12.2
%
   
12.2
%

(1)  Reflects the Company's US GAAP consolidated financial statements before pro forma adjustments related to the sale of the Dialysis and BioSentry Businesses on June 8, 2023, the sale of the PICCs and Midlines Businesses on February 15, 2024 and the discontinuation of the RadioFrequency Ablation and Syntrax products ("the Businesses") as of February 29, 2024, for the three months ended August 31, 2024.
(2) Reflects the elimination of revenues and expenses representing the operating results from the sales and discontinuation of the Businesses.

GROSS MARGIN BY PRODUCT CATEGORY

(in thousands)

   
Three Months Ended
             
         
As Reported (1)
   
Pro Forma
Adjustments (2)
   
Pro Forma
   
Actual
   
Pro Forma
 
   
Aug 31, 2025
   
Aug 31, 2024
   
Aug 31, 2024
   
Aug 31, 2024
   
% Change
   
% Change
 
   
(unaudited)
   
(unaudited)
             
Med Tech
 
$
21,922
   
$
17,697
   
$
   
$
17,697
     
23.9
%
   
23.9
%
Gross margin % of sales
   
62.2
%
   
63.3
%
           
63.3
%
               
                                                 
Med Device
 
$
19,935
   
$
19,027
   
$
11
   
$
19,038
     
4.8
%
   
4.7
%
Gross margin % of sales
   
49.3
%
   
48.1
%
           
48.2
%
               
                                                 
Total
 
$
41,857
   
$
36,724
   
$
11
   
$
36,735
     
14.0
%
   
13.9
%
Gross margin % of sales
   
55.3
%
   
54.4
%
           
54.4
%
               

(1)  Reflects the Company's US GAAP consolidated financial statements before pro forma adjustments related to the sale of the Dialysis and BioSentry Businesses on June 8, 2023, the sale of the PICCs and Midlines Businesses on February 15, 2024 and the discontinuation of the RadioFrequency Ablation and Syntrax products ("the Businesses") as of February 29, 2024, for the three months ended August 31, 2024.
(2) Reflects the elimination of revenues and expenses representing the operating results from the sales and discontinuation of the Businesses.

11

ANGIODYNAMICS, INC. AND SUBSIDIARIES
CONSOLIDATED BALANCE SHEETS
(in thousands)

   
Aug 31, 2025
   
May 31, 2025
 
   
(unaudited)
   
(audited)
 
Assets
           
Current assets:
           
Cash and cash equivalents
 
$
38,762
   
$
55,893
 
Accounts receivable, net
   
42,643
     
42,890
 
Inventories
   
62,255
     
62,006
 
Prepaid expenses and other
   
12,996
     
7,535
 
Total current assets
   
156,656
     
168,324
 
Property, plant and equipment, net
   
31,066
     
32,300
 
Other assets
   
9,540
     
10,404
 
Intangible assets, net
   
68,380
     
69,116
 
Total assets
 
$
265,642
   
$
280,144
 
Liabilities and stockholders' equity
               
Current liabilities:
               
Accounts payable
 
$
31,882
   
$
33,291
 
Accrued liabilities
   
27,657
     
35,518
 
Other current liabilities
   
8,743
     
7,388
 
Total current liabilities
   
68,282
     
76,197
 
Deferred income taxes
   
4,268
     
4,073
 
Other long-term liabilities
   
14,237
     
16,904
 
Total liabilities
   
86,787
     
97,174
 
Stockholders' equity
   
178,855
     
182,970
 
Total Liabilities and Stockholders' Equity
 
$
265,642
   
$
280,144
 

12

ANGIODYNAMICS, INC. AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF CASH FLOWS
(in thousands)

   
Three Months Ended
 
   
Aug 31, 2025
   
Aug 31, 2024
 
   
(unaudited)
 
Cash flows from operating activities:
           
Net loss
 
$
(10,903
)
 
$
(12,798
)
Adjustments to reconcile net loss to net cash used in operating activities:
               
Depreciation and amortization
   
6,020
     
6,785
 
Non-cash lease expense
   
445
     
494
 
Stock based compensation
   
4,470
     
3,205
 
Change in fair value of contingent consideration
   
     
76
 
Deferred income taxes
   
(16
)
   
(339
)
Change in accounts receivable allowances
   
108
     
270
 
Fixed and intangible asset impairments and disposals
   
(27
)
   
20
 
Other
   
264
     
121
 
Changes in operating assets and liabilities:
               
Accounts receivable
   
139
     
3,784
 
Inventories
   
(192
)
   
(4,053
)
Prepaid expenses and other
   
(5,525
)
   
(836
)
Accounts payable, accrued and other liabilities
   
(10,697
)
   
(14,982
)
Net cash used in operating activities
   
(15,914
)
   
(18,253
)
Cash flows from investing activities:
               
Additions to property, plant and equipment
   
(731
)
   
(1,092
)
Additions to placement and evaluation units
   
(820
)
   
(1,313
)
Net cash used in investing activities
   
(1,551
)
   
(2,405
)
Cash flows from financing activities:
               
Principal payments on finance arrangements
   
(91
)
   
 
Repurchase of common stock
   
     
(552
)
Proceeds from exercise of stock options and employee stock purchase plan
   
234
     
43
 
Net cash provided by (used in) financing activities
   
143
     
(509
)
Effect of exchange rate changes on cash and cash equivalents
   
191
     
116
 
Decrease in cash and cash equivalents
   
(17,131
)
   
(21,051
)
Cash and cash equivalents at beginning of period
   
55,893
     
76,056
 
Cash and cash equivalents at end of period
 
$
38,762
   
$
55,005
 


13


Exhibit 99.2

 First Quarter FY 2026Earnings Results  October 2, 2025 
 

 Forward looking statements   2  Notice Regarding Forward-Looking Statements  This presentation contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements regarding AngioDynamics’ expected future financial position, results of operations, cash flows, business strategy, budgets, projected costs, capital expenditures, products, competitive positions, growth opportunities, plans and objectives of management for future operations, as well as statements that include the words such as “expects,” “reaffirms,” “intends,” “anticipates,” “plans,” “projects,” “believes,” “seeks,” “estimates,” “optimistic,” or variations of such words and similar expressions, are forward-looking statements. These forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties. Investors are cautioned that actual events or results may differ materially from AngioDynamics’ expectations, expressed or implied. Factors that may affect the actual results achieved by AngioDynamics include, without limitation, the scale and scope of the COVID-19 global pandemic, the ability of AngioDynamics to develop its existing and new products, technological advances and patents attained by competitors, infringement of AngioDynamics’ technology or assertions that AngioDynamics’ technology infringes the technology of third parties, the ability of AngioDynamics to effectively compete against competitors that have substantially greater resources, future actions by the FDA or other regulatory agencies, domestic and foreign health care reforms and government regulations, results of pending or future clinical trials, overall economic conditions (including inflation, tariffs, labor shortages and supply chain challenges including the cost and availability of raw materials), the results of on-going litigation, challenges with respect to third-party distributors or joint venture partners or collaborators, the results of sales efforts, the effects of product recalls and product liability claims, changes in key personnel, the ability of AngioDynamics to execute on strategic initiatives, the effects of economic, credit and capital market conditions, general market conditions, market acceptance, foreign currency exchange rate fluctuations, the effects on pricing from group purchasing organizations and competition, the ability of AngioDynamics to obtain regulatory clearances or approval of its products, or to integrate acquired businesses, as well as the risk factors listed from time to time in AngioDynamics’ SEC filings, including but not limited to its Annual Report on Form 10-K for the year ended May 31, 2025. AngioDynamics does not assume any obligation to publicly update or revise any forward-looking statements for any reason.  Notice Regarding Non-GAAP Financial Measures  Management uses non-GAAP measures to establish operational goals and believes that non-GAAP measures may assist investors in analyzing the underlying trends in AngioDynamics’ business over time. Investors should consider these non-GAAP measures in addition to, not as a substitute for or as superior to, financial reporting measures prepared in accordance with GAAP. In this presentation, AngioDynamics has reported pro forma results, adjusted EBITDA (income before interest, taxes, depreciation and amortization and stock-based compensation); adjusted net income and adjusted earnings per share. Management uses these measures in its internal analysis and review of operational performance. Management believes that these measures provide investors with useful information in comparing AngioDynamics’ performance over different periods. By using these non-GAAP measures, management believes that investors get a better picture of the performance of AngioDynamics’ underlying business. Management encourages investors to review AngioDynamics’ financial results prepared in accordance with GAAP to understand AngioDynamics’ performance taking into account all relevant factors, including those that may only occur from time to time but have a material impact on AngioDynamics’ financial results. Please see the tables that follow for a reconciliation of non-GAAP measures to measures prepared in accordance with GAAP. 
 

 3  FY Q1 2026 Key Takeaways  Continued commercial and operational execution positions AngioDynamics to drive accelerated, profitable growth moving forward.  Continued Commercial Execution – Fiscal Q1 FY 2026  Total  +12.2%   YoY Revenue Growth*  Med Tech  +26.1%   Med Device  +2.3%   Auryon  +20.1%   Med Tech YoY Revenue Growth*  Mech Thrombectomy  +41.2%   NanoKnife Probes  +31.3%    Focus on Profitability  Balance Sheet Strength  Ended quarter with $38.8M in Cash  Currently have zero debt with flexibility of revolving line of credit  Cash utilization of ~$17M in the quarter, ahead of prior guidance  Pro forma Adjusted EBITDA of $2.2M, an improvement of $2.3M from Q1 FY25  Continued Execution  Net sales of $75.7M, +12.2% YoY growth  Med Tech segment sales of $35.3M, +26.1% YoY growth  Med Device segment sales of $40.4M, +2.3% YoY growth  *All growth rates are pro forma 
 

 4  Demonstrated Med Tech Growth Execution  4  Med Tech  ~22% of Total  Med Tech  ~47% of Total  +14% - 16%  *Guidance issued in conjunction with fiscal Q1 2026 earnings call on Oct 2, 2025  Med Tech 5yr CAGR: +25% 
 

 5  Q1 FY 2026 Financial Snapshot  +2.3%   Pro Forma Growth  +26.1%  Pro Forma Growth  Segment Revenue Contribution  Segment Gross Margin  49.3%  62.2%  Med Device  Med Tech 
 

 6  Med Tech - Auryon  Combination of Auryon’s best-in-class technology and our commercial strategy have positioned Auryon as a consistently high-growth platform being supported by continued investment in use cases  Period  Sales  YoY Growth  Q1 2026  $16.5M  20.1%  Continued penetration into hospital setting provides higher ASPs and improving margins  Growing contribution from International following CE Mark in Sept 2024  AMBITION BTK RCT and Registry ongoing, first patient enrolled 
 

 7  Med Tech – Thrombus Management  Combination of AngioVac and AlphaVac represent a strong, highly competitive mechanical thrombectomy portfolio which continues to take market share driven by expanded joint commercial strategy  AngioVac  ~37% YoY growth in Q1  AlphaVac  ~52% YoY growth in Q1 driven by growth in PE  First patient enrolled in E.U. based RECOVER-AV trial  Q1 2026  Sales  YoY Growth  AngioVac  $8.0M  37.1%  AlphaVac  $3.3M  52.3%  Total Mech Thromb.  $11.3M  41.2%  Unifuse  $1.1M  (9.1)%  Total Thrombus Mgmt.  $12.4M  34.7% 
 

 8  Med Tech - NanoKnife  Adoption has continued to accelerate within Prostate as this novel therapy gains traction following receipt of FDA clearance in Dec 2025  Accelerating demand for NanoKnife for prostate driving increased adoption  Received Prostate Tissue CPT Category 1 Code (effective Jan. 1, 2026), which is expected to streamline reimbursement for healthcare providers conducting irreversible electroporation (IRE) ablation procedures  Received Pancreas procedures CPT level I code (effective Jan. 1, 2027) - IRE code approval expands NanoKnife applicability   Q1 2026  Sales  YoY Growth  Disposables  $5.4M  31.3%  Capital  $1.1M  8.0%  Total  $6.4M  26.7% 
 

 9  Compelling FY 2026 Financial Outlooksupported by balance sheet strength  *Guidance was issued in conjunction with fiscal Q1 2026 earnings call on Oct 2, 2025  +14 - 16%  Med Tech  Metric  Action  Current Guidance  Prior Guidance  Net Sales  Increased  $308 - $313M  $305 - $310M  Med Tech Net Sales Growth  Increased  +14 – 16%  +12 – 15%  Med Device Net Sales Growth  Unchanged  Flat  Flat  Gross Margin  Unchanged  53.5 – 55.5%  53.5 – 55.5%  Adjusted EBITDA  Increased  +$6.0 - $10.0M  +$3.0M - $8.0M  Adjusted EPS  Increased  ($0.33) – ($0.23)  ($0.35) – ($0.25)  Free Cash Flow  Unchanged  Positive for Full Year  Positive for Full Year  Flat  Med Device  Balance Sheet Strength Supports Long Term Strategy  FY 2026 Financial Guidance*  $38.8M in Cash at Aug 31, 2025  Zero debt on balance sheet with flexibility from revolving line of credit 
 

 10  Appendix 
 

 11  Reconciliation of GAAP to Non-GAAP Pro Forma Results for the Consolidated Income Statements (in thousand, except per share data) 
 

 12  Reconciliation of GAAP Net Loss to Non-GAAP Adjusted Net Loss and EPS and Pro Forma Adjusted Net Loss and EPS (in thousands, except per share data)  Reconciliation of Net Loss to Adjusted EBITDA and Pro Forma Adjusted EBITDA  (in thousands, except per share data) 
 

 13  Detail of “Acquisition, Restructuring and Other Items, net” 
 

 14  Reconciliation of GAAP to Non-GAAP Pro Forma Results for Sales and Gross Margin by Product Category   (in thousands)