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AngioDynamics Reports Fiscal Year 2025 First Quarter Financial Results

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AngioDynamics (NASDAQ: ANGO) reported financial results for Q1 FY2025, ending August 31, 2024. Net sales reached $67.5 million, a 1.1% increase year-over-year. Med Tech sales grew 8.7% to $28.0 million, while Med Device sales decreased 3.6% to $39.5 million. The company reported a GAAP loss per share of $0.31 and an adjusted loss per share of $0.11.

Key highlights include:

  • Submission for FDA 510(k) clearance for NanoKnife's Prostate Tissue indication
  • CE Mark Approval in Europe for the Auryon System
  • Initiation of RECOVER-AV Clinical Trial in Europe for AlphaVac

For FY2025, AngioDynamics expects net sales between $282-$288 million, representing 4.2%-6.4% growth over FY2024 pro forma revenue. The company anticipates an adjusted EBITDA loss of $2.5 million to $0 and an adjusted loss per share of $0.38 to $0.42.

AngioDynamics (NASDAQ: ANGO) ha riportato i risultati finanziari per il primo trimestre dell'anno fiscale 2025, terminato il 31 agosto 2024. Le vendite nette hanno raggiunto 67,5 milioni di dollari, con un aumento dell'1,1% rispetto all'anno precedente. Le vendite nel settore Med Tech sono cresciute dell'8,7%, arrivando a 28,0 milioni di dollari, mentre le vendite di Med Device sono diminuite del 3,6%, attestandosi a 39,5 milioni di dollari. L'azienda ha riportato una perdita per azione GAAP di 0,31 dollari e una perdita per azione rettificata di 0,11 dollari.

I punti salienti includono:

  • Presentazione per l'approvazione FDA 510(k) per l'indicazione del tessuto prostatico del NanoKnife
  • Approvazione del Marchio CE in Europa per il Sistema Auryon
  • Inizio dello studio clinico RECOVER-AV in Europa per AlphaVac

Per l'anno fiscale 2025, AngioDynamics prevede vendite nette comprese tra 282 e 288 milioni di dollari, rappresentando una crescita del 4,2%-6,4% rispetto al fatturato pro forma del FY2024. L'azienda prevede una perdita EBITDA rettificata compresa tra 2,5 milioni di dollari e 0 e una perdita per azione rettificata di 0,38-0,42 dollari.

AngioDynamics (NASDAQ: ANGO) reportó resultados financieros para el primer trimestre del año fiscal 2025, que terminó el 31 de agosto de 2024. Las ventas netas alcanzaron 67,5 millones de dólares, un aumento del 1,1% en comparación con el año anterior. Las ventas de Med Tech crecieron un 8,7% a 28,0 millones de dólares, mientras que las ventas de Med Device disminuyeron un 3,6% a 39,5 millones de dólares. La empresa reportó una pérdida por acción GAAP de 0,31 dólares y una pérdida por acción ajustada de 0,11 dólares.

Los puntos destacados incluyen:

  • Solicitud de aprobación de la FDA 510(k) para la indicación de tejido prostático de NanoKnife
  • Aprobación de CE Mark en Europa para el sistema Auryon
  • Inicio del ensayo clínico RECOVER-AV en Europa para AlphaVac

Para el año fiscal 2025, AngioDynamics espera ventas netas entre 282 y 288 millones de dólares, lo que representa un crecimiento del 4,2%-6,4% en comparación con los ingresos pro forma del FY2024. La empresa anticipa una pérdida EBITDA ajustada de entre 2,5 millones de dólares y 0, así como una pérdida por acción ajustada de entre 0,38 y 0,42 dólares.

AngioDynamics (NASDAQ: ANGO)는 2025 회계연도 1분기 결과를 보고했습니다. 해당 분기는 2024년 8월 31일로 종료되었습니다. 순매출은 6,750만 달러에 도달했으며, 전년 대비 1.1% 증가했습니다. 의료 기술(Med Tech) 매출은 8.7% 증가하여 2,800만 달러를 기록했고, 의료 기기(Med Device) 매출은 3.6% 감소하여 3,950만 달러에 이르렀습니다. 회사는 주당 GAAP 손실 0.31 달러조정된 주당 손실 0.11 달러를 보고했습니다.

주요 하이라이트는 다음과 같습니다:

  • NanoKnife의 전립선 조직 적응증에 대한 FDA 510(k) 승인 신청
  • Auryon 시스템에 대한 유럽 CE 마크 승인
  • AlphaVac에 대한 유럽 내 RECOVER-AV 임상 시험 시작

2025 회계연도에 대해 AngioDynamics는 순매출이 2억 8,200만에서 2억 8,800만 달러 사이일 것으로 예상하며, 이는 2024 회계연도의 프로 포르마 수익 대비 4.2%-6.4% 성장에 해당합니다. 회사는 조정된 EBITDA 손실이 250만 달러에서 0로, 조정된 주당 손실이 0.38달러에서 0.42달러 사이일 것으로 예상하고 있습니다.

AngioDynamics (NASDAQ: ANGO) a rapporté les résultats financiers pour le premier trimestre de l'exercice 2025, se terminant le 31 août 2024. Les ventes nettes ont atteint 67,5 millions de dollars, soit une augmentation de 1,1% par rapport à l'année précédente. Les ventes dans le secteur de Med Tech ont augmenté de 8,7% pour atteindre 28,0 millions de dollars, tandis que les ventes de Med Device ont diminué de 3,6% pour s'établir à 39,5 millions de dollars. La société a rapporté une perte par action GAAP de 0,31 dollar et une perte par action ajustée de 0,11 dollar.

Parmi les points clés, on note :

  • Soumission pour l'autorisation FDA 510(k) pour l'indication des tissus prostatiques du NanoKnife
  • Approbation du marquage CE en Europe pour le système Auryon
  • Lancement de l'essai clinique RECOVER-AV en Europe pour AlphaVac

Pour l'exercice 2025, AngioDynamics s'attend à des ventes nettes comprises entre 282 et 288 millions de dollars, représentant une croissance de 4,2%-6,4% par rapport aux revenus pro forma de l'exercice 2024. La société prévoit une perte EBITDA ajustée de 2,5 millions de dollars à 0 et une perte par action ajustée de 0,38 à 0,42 dollars.

AngioDynamics (NASDAQ: ANGO) berichtete über die finanziellen Ergebnisse für das erste Quartal des Geschäftsjahres 2025, das am 31. August 2024 endete. Der Nettoumsatz betrug 67,5 Millionen Dollar, was einem Anstieg von 1,1% im Vergleich zum Vorjahr entspricht. Die Umsätze im Bereich Med Tech stiegen um 8,7% auf 28,0 Millionen Dollar, während die Umsätze im Bereich Med Device um 3,6% auf 39,5 Millionen Dollar sanken. Das Unternehmen meldete einen GAAP-Verlust pro Aktie von 0,31 Dollar und einen bereinigten Verlust pro Aktie von 0,11 Dollar.

Zu den wichtigsten Highlights gehören:

  • Einreichung zur FDA 510(k)-Freigabe für die Anzeichen von Prostatagewebe des NanoKnife
  • CE-Kennzeichnung für das Auryon-System in Europa
  • Start der klinischen Studie RECOVER-AV in Europa für AlphaVac

Für das Geschäftsjahr 2025 erwartet AngioDynamics einen Nettoumsatz zwischen 282 und 288 Millionen Dollar, was einem Wachstum von 4,2%-6,4% im Vergleich zu den pro forma Einnahmen des Geschäftsjahres 2024 entspricht. Das Unternehmen rechnet mit einem bereinigten EBITDA-Verlust zwischen 2,5 Millionen Dollar und 0 sowie einem bereinigten Verlust pro Aktie von 0,38 bis 0,42 Dollar.

Positive
  • Med Tech net sales increased by 8.7% to $28.0 million
  • Auryon sales grew 24.9% to $13.7 million
  • AlphaVac sales increased 21.1% to $2.2 million
  • U.S. net sales grew 6.2% to $59.5 million
  • Submitted FDA 510(k) clearance for NanoKnife's Prostate Tissue indication
  • Received CE Mark Approval in Europe for the Auryon System
  • Initiated RECOVER-AV Clinical Trial in Europe for AlphaVac
Negative
  • GAAP net loss of $12.8 million, or $0.31 per share
  • Adjusted net loss of $4.4 million, or $0.11 per share
  • Med Device net sales decreased 3.6% to $39.5 million
  • International net sales decreased 25.4% to $8.0 million
  • NanoKnife sales decreased 6.9% to $5.1 million
  • Gross margin decreased 40 basis points year-over-year to 54.4%
  • Used $18.3 million in operating cash during Q1 FY2025

Insights

AngioDynamics' Q1 FY2025 results show mixed performance. The company reported $67.5 million in net sales, a modest 1.1% increase year-over-year on a pro forma basis. The Med Tech segment was the bright spot, growing 8.7% to $28 million, driven by strong performances from Auryon (24.9% growth) and AlphaVac (21.1% growth). However, the Med Device segment declined 3.6% to $39.5 million.

The company's gross margin slightly decreased to 54.4%, down 40 basis points year-over-year. The GAAP loss per share of $0.31 and adjusted loss per share of $0.11 indicate ongoing profitability challenges. Cash position decreased from $76.1 million to $55 million during the quarter, reflecting significant cash burn.

Looking ahead, AngioDynamics maintains its FY2025 guidance, projecting net sales of $282-288 million and an adjusted EBITDA loss of $2.5-0 million. While the company sees FY2025 as an inflection point, investors should closely monitor cash burn and the path to profitability.

AngioDynamics' Q1 results highlight the company's strategic focus on its Med Tech segment, particularly the Auryon and AlphaVac platforms. The Auryon peripheral atherectomy system's 24.9% growth is impressive, indicating strong market adoption. The recent CE Mark approval for Auryon in Europe opens up significant expansion opportunities in the $1.1 billion global PAD market.

The submission of PRESERVE study results for NanoKnife's prostate tissue indication is a important milestone. If approved, it could substantially broaden the system's application and market potential. However, the 6.9% decline in NanoKnife sales is a concern that needs addressing.

The initiation of the RECOVER-AV trial for AlphaVac in Europe demonstrates the company's commitment to expanding its evidence base and market presence in thrombectomy. This strategic move could strengthen AngioDynamics' position in the growing pulmonary embolism treatment market.

While the Med Tech segment shows promise, the decline in the Med Device segment suggests a need for portfolio optimization or revitalization strategies to ensure balanced growth across the business.

LATHAM, N.Y.--(BUSINESS WIRE)-- 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 ended August 31, 2024.

Fiscal Year 2025 First Quarter Highlights

 

Quarter Ended
August 31, 2024

Pro Forma* YoY Growth

Net Sales

$67.5 million

1.1%

Med Tech Net Sales

$28.0 million

8.7%

Med Device Net 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 in Europe for the Auryon System
  • Initiated RECOVER-AV Clinical Trial in Europe for AlphaVac

*Pro forma results exclude the Dialysis and BioSentry businesses divested in June 2023 and the PICC and Midline product portfolios divested in February 2024, as well as the discontinued Radiofrequency and Syntrax products in February 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," commented Jim Clemmer, President and Chief Executive Officer of AngioDynamics, 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 million in 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 million during 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 million in 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 million a year ago. International net sales were $8.0 million, a decrease of 25.4%, compared to $10.7 million a 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) million in the first quarter of fiscal 2024.

In the first quarter of fiscal 2025, the Company used $18.3 million in 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.

At August 31, 2024, the Company had $55.0 million in cash and cash equivalents compared to $76.1 million in cash and cash equivalents at May 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 the U.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 throughout the United States.

CE Mark Approval in Europe for the Auryon System

Prior to the end of the quarter AngioDynamics received European CE Mark approval for its Auryon Atherectomy System. This regulatory approval allows AngioDynamics to market the Auryon System in Europe for 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 in the 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 expands AngioDynamics' 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 in Europe. Following the successful APEX-AV study in the 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 $282 to $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 million to $0, compared to a pro forma adjusted EBITDA loss of $3.2 million in fiscal year 2024
  • Adjusted loss per share in the range of $0.38 to $0.42, compared to pro forma adjusted loss per share of $0.45 in fiscal year 2024

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 10, 2024 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 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 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.

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, 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, 2024. AngioDynamics does not assume any obligation to publicly update or revise any forward-looking statements for any reason.

In the United States, the NanoKnife System has received a 510(k) clearance by the Food and Drug Administration for use in the surgical ablation of soft tissue and is similarly approved for commercialization in Canada, the European Union and Australia. 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 Forma
Adjustments (2)

 

Pro Forma

 

As Reported (1)

 

Pro Forma
Adjustments (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 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 and 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's U.S. deferred tax assets and an effective tax rate of 23% for the periods ended August 31, 2024 and 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's U.S. deferred tax assets and an effective tax rate of 23% for the periods ended August 31, 2024 and 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 on January 5, 2024.
(3) Transition services agreements that were entered into with Merit and Spectrum.
(4) Expenses to relocate certain manufacturing lines out of Queensbury, NY.

ANGIODYNAMICS, INC. AND SUBSIDIARIES

NET SALES BY PRODUCT CATEGORY AND BY GEOGRAPHY

(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

 

% 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 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 and 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 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 and 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

 

 

Investors:

AngioDynamics, Inc.

Stephen Trowbridge, Executive Vice President & CFO

(518) 795-1408

Source: AngioDynamics, Inc.

FAQ

What were AngioDynamics' (ANGO) Q1 FY2025 net sales?

AngioDynamics reported net sales of $67.5 million for Q1 FY2025, representing a 1.1% increase year-over-year on a pro forma basis.

How did AngioDynamics' (ANGO) Med Tech segment perform in Q1 FY2025?

AngioDynamics' Med Tech segment net sales grew 8.7% to $28.0 million in Q1 FY2025, driven by strong performance from Auryon and AlphaVac products.

What is AngioDynamics' (ANGO) financial guidance for FY2025?

For FY2025, AngioDynamics expects net sales between $282-$288 million, an adjusted EBITDA loss of $2.5 million to $0, and an adjusted loss per share of $0.38 to $0.42.

What regulatory milestones did AngioDynamics (ANGO) achieve in Q1 FY2025?

AngioDynamics submitted for FDA 510(k) clearance for NanoKnife's Prostate Tissue indication and received CE Mark Approval in Europe for the Auryon System.

How did AngioDynamics' (ANGO) gross margin perform in Q1 FY2025?

AngioDynamics' gross margin for Q1 FY2025 was 54.4%, which was 40 basis points lower compared to Q1 FY2024.

AngioDynamics, Inc.

NASDAQ:ANGO

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ANGO Stock Data

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Medical Instruments & Supplies
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