AngioDynamics Reports Fiscal Year 2025 First Quarter Financial Results

ANGO 10.03.2024

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Recent News

  • 01.16.2025 - 43rd Annual J.P. Morgan Healthcare Conference
  • 01.13.2025 - AngioDynamics Announces Publication of APEX-AV Trial Results in JSCAI
  • 01.08.2025 - Virtual NanoKnife Investor Event

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  • 01.17.2025 - 4 Statement of changes in beneficial ownership of securities
  • 01.16.2025 - 8-K Current report
  • 01.16.2025 - 144 Report of proposed sale of securities

LATHAM, N.Y.--(BUSINESS WIRE)--Oct. 3, 2024--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 2025, which endedAugust 31, 2024.

Fiscal Year 2025 First Quarter Highlights

Quarter EndedAugust 31, 2024

Pro Forma* YoY Growth

Net Sales

$67.5 million

1.1%

Med TechNet Sales

$28.0 million

8.7%

Med DeviceNet Sales

$39.5 million

(3.6)%

  • GAAP gross margin of 54.4%
  • GAAP loss per share of$0.31
  • Adjusted loss per share of$0.11
  • Submitted for FDA 510(k) clearance for Prostate Tissue indication for NanoKnife
  • Received CE Mark Approval inEuropefor the Auryon System
  • Initiated RECOVER-AV Clinical Trial inEuropefor AlphaVac

*Pro forma results exclude the Dialysis and BioSentry businesses divested inJune 2023and the PICC and Midline product portfolios divested inFebruary 2024, as well as the discontinued Radiofrequency and Syntrax products inFebruary 2024.

"We are pleased with our strong start to fiscal year 2025, particularly in our Med Tech segment, with Auryon and AlphaVac both delivering over 20% growth in the quarter," commentedJim Clemmer, President and Chief Executive Officer ofAngioDynamics, Inc."We continue to view 2025 as an inflection point in the trajectory of our business. We expect to continue to deliver strong revenue growth within our Med Tech business as we execute on key commercial initiatives. We remain focused on executing our growth strategy and advancing our innovative product portfolio."

Fiscal Year 2025 First Quarter Financial Results

Unless otherwise noted, all financial metrics and growth rates presented below are on a pro forma basis.

Net sales for the first quarter of fiscal year 2025 were$67.5 million, an increase of 1.1% compared to the prior-year quarter.

Med Tech net sales were$28.0 million, an 8.7% increase from$25.7 millionin the prior-year period. Med Tech includes the Auryon peripheral atherectomy platform, the thrombus management platform, which includes the AlphaVac and AngioVac mechanical thrombectomy systems, and the NanoKnife irreversible electroporation platform.

Growth was driven by Auryon sales during the quarter of$13.7 million, which increased 24.9% and AlphaVac sales of$2.2 million, an increase of 21.1% over the prior year. NanoKnife sales were$5.1 millionduring the quarter, a decrease of 6.9% compared to the prior year period, primarily due to the timing of international orders during last year.

Med Device net sales were$39.5 million, a decrease of 3.6% compared to$41.0 millionin the prior-year period.U.S.net sales of Med Device products grew 2.1% during the first quarter compared to last year.

U.S.net sales in the first quarter of fiscal 2025 were$59.5 million, an increase of 6.2% from$56.0 milliona year ago. International net sales were$8.0 million, a decrease of 25.4%, compared to$10.7 milliona year ago, primarily due to the timing of international orders during last year.

Gross margin for the first quarter of fiscal 2025 was 54.4%, which was 40 basis points down compared to the first quarter of fiscal 2024, and 10 basis points sequentially up from 54.3% in the fourth quarter of fiscal 2024.

Gross margin for the Med Tech business was 63.3%, a decrease of 160 basis points from the first quarter of fiscal 2024 due to increased capital placements and inflationary costs. Gross margin for the Med Device business was 48.2%, a decrease of 40 basis points compared to the first quarter of fiscal 2024 due to inflationary pressures and costs associated with the transition to outsourced manufacturing.

The Company recorded a GAAP net loss of$12.8 million, or a loss per share of$0.31, in the first quarter of fiscal 2025. Excluding the items shown in the non-GAAP reconciliation table below, adjusted net loss for the first quarter of fiscal 2025 was$4.4 million, or a loss per share of$0.11. This compares to an adjusted net loss during the fiscal first quarter of 2024 of$6.2 million, or a loss per share of$0.16.

Adjusted EBITDA in the first quarter of fiscal 2025, excluding the items shown in the non-GAAP reconciliation table below, was$(0.2) million, compared to$(1.1) millionin the first quarter of fiscal 2024.

In the first quarter of fiscal 2025, the Company used$18.3 millionin operating cash. The Company’s first fiscal quarter has historically exhibited the highest utilization of cash and the first quarter of fiscal 2025 was in line with the Company’s expectations.

AtAugust 31, 2024, the Company had$55.0 millionin cash and cash equivalents compared to$76.1 millionin cash and cash equivalents atMay 31, 2024.

NanoKnife System's PRESERVE Study Results Submitted for FDA 510(k) Clearance

In September, the Company submitted results from its Pivotal Study of the NanoKnife System for Ablation of Prostate Tissue in an Intermediate-Risk Patient Population (PRESERVE) to theU.S. Food and Drug Administration(FDA) for 510(k) indication of its NanoKnife System in the ablation of prostate tissue in an intermediate-risk population. The comprehensive study enrolled and treated 121 patients across 17 facilities throughoutthe United States.

CE Mark Approval inEuropefor the Auryon System

Prior to the end of the quarterAngioDynamicsreceived European CE Mark approval for its Auryon Atherectomy System. This regulatory approval allowsAngioDynamicsto market the Auryon System inEuropefor the treatment of Peripheral Artery Disease (PAD), including Critical Limb Ischemia (CLI) and In-Stent Restenosis (ISR). The Auryon System uses solid-state laser technology to treat PAD lesions and occlusions. It has been cleared by the FDA since 2020 and has treated over 50,000 patients inthe United States. The system is designed to treat lesions of various types, lengths, and locations, both above and below the knee. This CE Mark approval expandsAngioDynamics'potential market reach, as the global PAD market is valued at$1.1 billion.

RECOVER-AV Clinical Trial

Subsequent to the end of the first fiscal quarter, the Company initiated its RECOVER-AV clinical trial, marking a significant step in evaluating the AlphaVac F1885 System for treating acute, intermediate-risk pulmonary embolism (PE) in the European market. This multi-center, multi-national study will assess the efficacy, safety, and long-term functional outcomes of the system across up to 20 hospital sites inEurope. Following the successful APEX-AV study inthe United States, RECOVER-AV aims to further demonstrate the system's capabilities in a region where PE prevalence is notably higher. The trial will track patient outcomes over a 12-month period, focusing on key efficacy and safety endpoints.

Fiscal Year 2025 Financial Guidance

For fiscal year 2025, the Company continues to expect:

  • Net sales to be in the range of$282to$288 million, representing growth of between 4.2% – 6.4% over fiscal 2024 pro forma revenue of$270.7 million
  • Med Tech net sales are expected to grow in the range of 10% to 12%
  • Med Device net sales are expected to grow in the range of 1% to 3%
  • Gross margin to be approximately 52% to 53%
  • Adjusted EBITDA loss of$2.5 millionto$0, compared to a pro forma adjusted EBITDA loss of$3.2 millionin fiscal year 2024
  • Adjusted loss per share in the range of$0.38to$0.42, compared to pro forma adjusted loss per share of$0.45in fiscal year 2024

Conference Call

The Company’s management will host a conference call at8:00 a.m. ETthe 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 theAngioDynamicswebsite atwww.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, untilThursday, October 10, 2024at11:59 PM ET. To hear this recording, dial 1-844-512-2921 (domestic) or +1-412-317-6671 (international) and enter the passcode 13748896.

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 inAngioDynamics'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,AngioDynamicshas 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 comparingAngioDynamics'performance over different periods. By using these non-GAAP measures, management believes that investors get a better picture of the performance ofAngioDynamics'underlying business. Management encourages investors to reviewAngioDynamics'financial results prepared in accordance with GAAP to understandAngioDynamics'performance taking into account all relevant factors, including those that may only occur from time to time but have a material impact onAngioDynamics'financial results. Please see the tables that follow for a reconciliation of non-GAAP measures to measures prepared in accordance with GAAP.

AboutAngioDynamics, Inc.

AngioDynamicsis 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, visitwww.angiodynamics.com.

Safe Harbor

This release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements regardingAngioDynamics'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 fromAngioDynamics'expectations, expressed or implied. Factors that may affect the actual results achieved byAngioDynamicsinclude, without limitation, the scale and scope of the COVID-19 global pandemic, the ability ofAngioDynamicsto develop its existing and new products, technological advances and patents attained by competitors, infringement ofAngioDynamics'technology or assertions thatAngioDynamics'technology infringes the technology of third parties, the ability ofAngioDynamicsto 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, 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 ofAngioDynamicsto 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 ofAngioDynamicsto obtain regulatory clearances or approval of its products, or to integrate acquired businesses, as well as the risk factors listed from time to time inAngioDynamics'SECfilings, including but not limited to its Annual Report on Form 10-K for the year endedMay 31, 2024.AngioDynamicsdoes not assume any obligation to publicly update or revise any forward-looking statements for any reason.

Inthe United States, the NanoKnife System has received a 510(k) clearance by theFood and Drug Administrationfor use in the surgical ablation of soft tissue and is similarly approved for commercialization inCanada, theEuropean UnionandAustralia. The NanoKnife System has not been cleared for the treatment or therapy of a specific disease or condition.

ANGIODYNAMICS, INC.AND SUBSIDIARIES

CONSOLIDATED INCOME STATEMENTS

(in thousands, except per share data)

Three Months Ended

Three Months Ended

Actual(1)

Pro FormaAdjustments(2)

Pro Forma

As Reported(1)

Pro FormaAdjustments(2)

Pro Forma

Aug 31, 2024

Aug 31, 2024

Aug 31, 2024

Aug 31, 2023

Aug 31, 2023

Aug 31, 2023

(unaudited)

(unaudited)

Net sales

$

67,491

9

$

67,500

$

78,679

(11,935

)

$

66,744

Cost of sales (exclusive of intangible amortization)

30,767

(2

)

30,765

38,619

(8,482

)

30,137

Gross profit

36,724

11

36,735

40,060

(3,453

)

36,607

% of net sales

54.4

%

54.4

%

50.9

%

54.8

%

Operating expenses

Research and development

6,285

—

6,285

7,941

(207

)

7,734

Sales and marketing

25,605

—

25,605

27,368

(1,487

)

25,881

General and administrative

10,975

—

10,975

10,856

(1

)

10,855

Amortization of intangibles

2,570

—

2,570

3,625

(964

)

2,661

Change in fair value of contingent consideration

76

—

76

(130

)

—

(130

)

Acquisition, restructuring and other items, net

4,311

154

4,465

3,212

(22

)

3,190

Total operating expenses

49,822

154

49,976

52,872

(2,681

)

50,191

Gain on sale of assets

—

—

—

47,842

(47,842

)

—

Operating income (loss)

(13,098

)

(143

)

(13,241

)

35,030

(48,614

)

(13,584

)

Interest income, net

606

—

606

119

—

119

Other expense, net

(173

)

—

(173

)

(288

)

—

(288

)

Total other income (expense), net

433

—

433

(169

)

—

(169

)

Income (loss) before income tax benefit

(12,665

)

(143

)

(12,808

)

34,861

(48,614

)

(13,753

)

Income tax expense (benefit)

133

—

133

(11,023

)

—

(11,023

)

Net income (loss)

$

(12,798

)

$

(143

)

$

(12,941

)

$

45,884

$

(48,614

)

$

(2,730

)

Earnings (loss) per share

Basic

$

(0.31

)

$

(0.32

)

$

1.15

$

(0.07

)

Diluted

$

(0.31

)

$

(0.32

)

$

1.15

$

(0.07

)

Weighted average shares outstanding

Basic

40,653

40,653

39,842

39,842

Diluted

40,653

40,653

39,968

39,842

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

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

ANGIODYNAMICS, INC.AND SUBSIDIARIES

GAAP TO NON-GAAP RECONCILIATION

(in thousands, except per share data)

Reconciliation of Net Income (Loss) to non-GAAP Adjusted Net Loss:

Three Months Ended

Aug 31, 2024

Aug 31, 2023

(unaudited)

Net income (loss)

$

(12,798

)

$

45,884

Amortization of intangibles

2,570

3,625

Change in fair value of contingent consideration

76

(130

)

Acquisition, restructuring and other items, net(1)

4,311

3,212

Gain on sale of assets

—

(47,842

)

Tax effect of non-GAAP items(2)

1,446

(9,580

)

Adjusted net loss

$

(4,395

)

$

(4,831

)

Reconciliation of Diluted Earnings (Loss) Per Share to non-GAAP Adjusted Diluted Loss Per Share:

Three Months Ended

Aug 31, 2024

Aug 31, 2023

(unaudited)

Diluted earnings (loss) per share

$

(0.31

)

$

1.15

Amortization of intangibles

0.06

0.09

Change in fair value of contingent consideration

0.00

0.00

Acquisition, restructuring and other items, net(1)

0.10

0.08

Gain on sale of assets

—

(1.20

)

Tax effect of non-GAAP items(2)

0.04

(0.24

)

Adjusted diluted loss per share

$

(0.11

)

$

(0.12

)

Adjusted diluted sharecount(3)

40,653

39,842

(1) Includes costs related to merger and acquisition activities, restructuring, and unusual items, including asset impairments and write-offs, certain litigation, and other items.

(2) Adjustment to reflect the income tax provision on a non-GAAP basis has been calculated assuming no valuation allowance on the Company'sU.S.deferred tax assets and an effective tax rate of 23% for the periods endedAugust 31, 2024and 2023.

(3) Diluted shares may differ for non-GAAP measures as compared to GAAP due to a GAAP loss.

ANGIODYNAMICS, INC.AND SUBSIDIARIES

GAAP TO NON-GAAP RECONCILIATION (Continued)

(in thousands, except per share data)

Reconciliation of Net Income (Loss) to Adjusted EBITDA:

Three Months Ended

Aug 31, 2024

Aug 31, 2023

(unaudited)

Net income (loss)

$

(12,798

)

$

45,884

Income tax expense (benefit)

133

(11,023

)

Interest income, net

(606

)

(119

)

Depreciation and amortization

6,785

6,688

Change in fair value of contingent consideration

76

(130

)

Stock based compensation

3,205

4,144

Acquisition, restructuring and other items, net(1)

3,042

3,212

Gain on sale of assets

—

(47,842

)

Adjusted EBITDA

$

(163

)

$

814

Per diluted share:

Adjusted EBITDA

$

0.00

$

0.02

(1) Includes costs related to merger and acquisition activities, restructuring, and unusual items, including asset impairments and write-offs, certain litigation, and other items.

ANGIODYNAMICS, INC.AND SUBSIDIARIES

GAAP TO NON-GAAP RECONCILIATION

(in thousands, except per share data)

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

Pro Forma

Three Months Ended

Aug 31, 2024

Aug 31, 2023

(unaudited)

Pro forma net loss

$

(12,941

)

$

(2,730

)

Amortization of intangibles

2,570

2,661

Change in fair value of contingent consideration

76

(130

)

Acquisition, restructuring and other items, net(1)

4,465

3,190

Tax effect of non-GAAP items(2)

1,443

(9,176

)

Adjusted pro forma net loss

$

(4,387

)

$

(6,185

)

Reconciliation of Pro Forma Diluted Loss Per Share to Pro Forma Adjusted Diluted Loss Per Share:

Pro Forma

Three Months Ended

Aug 31, 2024

Aug 31, 2023

(unaudited)

Pro forma diluted loss per share

$

(0.32

)

$

(0.07

)

Amortization of intangibles

0.06

0.07

Change in fair value of contingent consideration

0.00

0.00

Acquisition, restructuring and other items, net(1)

0.11

0.08

Tax effect of non-GAAP items(2)

0.04

(0.24

)

Adjusted pro forma diluted loss per share

$

(0.11

)

$

(0.16

)

Adjusted diluted sharecount(3)

40,653

39,842

(1) Includes costs related to merger and acquisition activities, restructuring, and unusual items, including asset impairments and write-offs, certain litigation, and other items.

(2) Adjustment to reflect the income tax provision on a non-GAAP basis has been calculated assuming no valuation allowance on the Company'sU.S.deferred tax assets and an effective tax rate of 23% for the periods endedAugust 31, 2024and 2023.

(3) Diluted shares may differ for non-GAAP measures as compared to GAAP due to a GAAP loss.

ANGIODYNAMICS, INC.AND SUBSIDIARIES

GAAP TO NON-GAAP RECONCILIATION (Continued)

(in thousands, except per share data)

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

Pro Forma

Three Months Ended

Aug 31, 2024

Aug 31, 2023

(unaudited)

Pro forma net loss

$

(12,941

)

$

(2,730

)

Income tax expense (benefit)

133

(11,023

)

Interest income, net

(606

)

(119

)

Depreciation and amortization

6,785

5,682

Change in fair value of contingent consideration

76

(130

)

Stock based compensation

3,205

4,058

Acquisition, restructuring and other items, net(1)

3,196

3,190

Adjusted EBITDA

$

(152

)

$

(1,072

)

Per diluted share:

Adjusted EBITDA

$

0.00

$

(0.03

)

(1) Includes costs related to merger and acquisition activities, restructuring, and unusual items, including asset impairments and write-offs, certain litigation, and other items.

ANGIODYNAMICS, INC.AND SUBSIDIARIES

ACQUISITION, RESTRUCTURING, AND OTHER ITEMS, NET DETAIL

(in thousands)

Three Months Ended

(in thousands)

Aug 31, 2024

Aug 31, 2023

Legal(1)

$

507

$

1,817

Plant closure(2)

3,589

—

Transition service agreement(3)

(507

)

(145

)

Manufacturing relocation(4)

—

587

Other

722

953

Total

$

4,311

$

3,212

(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 onJanuary 5, 2024.
(3) Transition services agreements that were entered into with Merit and Spectrum.
(4) Expenses to relocate certain manufacturing lines out ofQueensbury, NY.

ANGIODYNAMICS, INC.AND SUBSIDIARIES

NET SALES BY PRODUCT CATEGORY AND BY GEOGRAPHY

(in thousands)

Three Months Ended

Three Months Ended

Actual(1)

Pro FormaAdj.(2)

Pro Forma

AsReported(1)

Pro FormaAdj.(2)

Pro Forma

Actual

Pro Forma

Aug 31,2024

Aug 31,2024

Aug 31,2024

Aug 31,2023

Aug 31,2023

Aug 31,2023

% Growth

Currency Impact

Constant Currency Growth

%Growth

Currency Impact

Constant Currency Growth

(unaudited)

(unaudited)

Net Sales

Med Tech

$

27,969

$

—

$

27,969

$

25,860

$

(131

)

$

25,729

8.2

%

8.7

%

Med Device

39,522

9

39,531

52,819

(11,804

)

41,015

(25.2

)%

(3.6

)%

$

67,491

$

9

$

67,500

$

78,679

$

(11,935

)

$

66,744

(14.2

)%

0.0

%

(14.2

)%

1.1

%

0.0

%

1.1

%

Net Sales

United States

$

59,481

$

10

$

59,491

$

64,399

$

(8,395

)

$

56,004

(7.6

)%

6.2

%

International

8,010

(1

)

8,009

14,280

(3,540

)

10,740

(43.9

)%

0.0

%

(43.9

)%

(25.4

)%

$

67,491

$

9

$

67,500

$

78,679

$

(11,935

)

$

66,744

(14.2

)%

0.0

%

(14.2

)%

1.1

%

0.0

%

1.1

%

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

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

GROSS PROFIT BY PRODUCT CATEGORY

(in thousands)

Three Months Ended

Three Months Ended

Actual(1)

Pro Forma

Adj.(2)

Pro Forma

As Reported(1)

Pro Forma

Adj.(2)

Pro Forma

Actual

Pro Forma

Aug 31,2024

Aug 31,2024

Aug 31,2024

Aug 31,2023

Aug 31,2023

Aug 31,2023

% Change

% Change

(unaudited)

(unaudited)

Med Tech

$

17,697

$

—

$

17,697

$

16,727

$

(39

)

$

16,688

5.8

%

6.0

%

Gross profit % of sales

63.3

%

63.3

%

64.7

%

64.9

%

Med Device

$

19,027

$

11

$

19,038

$

23,333

$

(3,414

)

$

19,919

(18.5

)%

(4.4

)%

Gross profit % of sales

48.1

%

48.2

%

44.2

%

48.6

%

Total

$

36,724

$

11

$

36,735

$

40,060

$

(3,453

)

$

36,607

(8.3

)%

0.3

%

Gross profit % of sales

54.4

%

54.4

%

50.9

%

54.8

%

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

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

ANGIODYNAMICS, INC.AND SUBSIDIARIES

CONSOLIDATED BALANCE SHEETS

(in thousands)

Aug 31, 2024

May 31, 2024

(unaudited)

(audited)

Assets

Current assets:

Cash and cash equivalents

$

55,005

$

76,056

Accounts receivable, net

39,563

43,610

Inventories

64,700

60,616

Prepaid expenses and other

13,326

12,971

Total current assets

172,594

193,253

Property, plant and equipment, net

34,377

35,666

Other assets

10,883

11,369

Intangible assets, net

75,774

77,383

Total assets

$

293,628

$

317,671

Liabilities and stockholders' equity

Current liabilities:

Accounts payable

$

31,272

$

37,751

Accrued liabilities

34,108

41,098

Current portion of contingent consideration

4,804

4,728

Other current liabilities

6,515

7,578

Total current liabilities

76,699

91,155

Deferred income taxes

4,626

4,852

Other long-term liabilities

15,721

16,078

Total liabilities

97,046

112,085

Stockholders' equity

196,582

205,586

Total Liabilities and Stockholders' Equity

$

293,628

$

317,671

ANGIODYNAMICS, INC.AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CASH FLOWS

(in thousands)

Three Months Ended

Aug 31, 2024

Aug 31, 2023

(unaudited)

Cash flows from operating activities:

Net income (loss)

$

(12,798

)

$

45,884

Adjustments to reconcile net income (loss) to net cash used in operating activities:

Depreciation and amortization

6,785

6,688

Non-cash lease expense

494

476

Stock based compensation

3,205

4,144

Gain on disposal of assets

—

(47,842

)

Transaction costs for disposition

—

(2,427

)

Change in fair value of contingent consideration

76

(130

)

Deferred income taxes

(339

)

(11,415

)

Change in accounts receivable allowances

270

(78

)

Fixed and intangible asset impairments and disposals

20

65

Write-off of other assets

—

869

Other

121

(9

)

Changes in operating assets and liabilities:

Accounts receivable

3,784

3,157

Inventories

(4,053

)

(4,574

)

Prepaid expenses and other

(836

)

(4,168

)

Accounts payable, accrued and other liabilities

(14,982

)

(16,539

)

Net cash used in operating activities

(18,253

)

(25,899

)

Cash flows from investing activities:

Additions to property, plant and equipment

(1,092

)

(791

)

Additions to placement and evaluation units

(1,313

)

(767

)

Proceeds from sale of assets

—

100,000

Net cash (used in) provided by investing activities

(2,405

)

98,442

Cash flows from financing activities:

Repayment of long-term debt

—

(50,000

)

Payment of acquisition related contingent consideration

—

(10,000

)

Repurchase of common stock

(552

)

—

Proceeds from exercise of stock options and employee stock purchase plan

43

410

Net cash used in financing activities

(509

)

(59,590

)

Effect of exchange rate changes on cash and cash equivalents

116

13

Increase (decrease) in cash and cash equivalents

(21,051

)

12,966

Cash and cash equivalents at beginning of period

76,056

44,620

Cash and cash equivalents at end of period

$

55,005

$

57,586

View source version onbusinesswire.com:https://www.businesswire.com/news/home/20241003678383/en/

Investors:AngioDynamics, Inc.Stephen Trowbridge, Executive Vice President & CFO(518) 795-1408

Source:AngioDynamics, Inc.

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