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Zomedica Announces Third Quarter 2025 Financial Results: Revenue up 16% to $8.1 Million with 67% Gross Margins and $54 Million in Liquidity to Support Growth

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Zomedica (OTCQB:ZOMDF) reported record third quarter results for the period ended September 30, 2025, with revenue up 16% to $8.1 million and a 67% gross margin. Diagnostics revenue rose 51% and new Development Services contributed $0.7M this quarter. Operating expenses fell $0.5M sequentially to $12.0M, driving a lower net loss of $6.1M and an improved Adjusted Non-GAAP EBITDA loss of $3.7M. The company ended the quarter with $54.4M in cash and securities and 979,949,668 shares outstanding.

Zomedica (OTCQB:ZOMDF) ha riportato risultati record nel terzo trimestre per il periodo terminato il 30 settembre 2025, con ricavi in aumento del 16% a 8,1 milioni di dollari e un margine lordo del 67%. I ricavi diagnostici sono aumentati del 51% e i nuovi Servizi di Sviluppo hanno contribuito per 0,7 milioni di dollari in questo trimestre. Le spese operative sono diminuite di 0,5 milioni di dollari rispetto al trimestre precedente, a 12,0 milioni, guidando una perdita netta ridotta di 6,1 milioni e una perdita EBITDA Adjusted Non-GAAP migliorata di 3,7 milioni. L'azienda ha terminato il trimestre con 54,4 milioni di dollari in contante e titoli e 979.949.668 azioni in circolazione.

Zomedica (OTCQB:ZOMDF) reportó resultados récord en el tercer trimestre para el periodo terminado el 30 de septiembre de 2025, con los ingresos crecieron un 16% a 8,1 millones de dólares y un margen bruto del 67%. Los ingresos de diagnóstico aumentaron un 51% y los Servicios de Desarrollo nuevos aportaron 0,7 millones de dólares en este trimestre. Los gastos operativos cayeron 0,5 millones de dólares secuencialmente a 12,0 millones, impulsando una menor pérdida neta de 6,1 millones y una pérdida ajustada de EBITDA no GAAP mejorada de 3,7 millones. La empresa terminó el trimestre con 54,4 millones de dólares en efectivo y valores y 979,949,668 acciones en circulación.

Zomedica (OTCQB:ZOMDF)는 2025년 9월 30일 종료된 기간에 대해 3분기 기록적인 실적을 발표했으며, 매출이 16% 증가하여 810만 달러, 총 이익률이 67%를 기록했습니다. 진단 매출은 51% 증가했고, 새로 도입된 개발 서비스는 이번 분기에 70만 달러를 기여했습니다. 운영비는 전분기 대비 50만 달러 감소하여 1,200만 달러가 되었고, 순손실은 610만 달러로 감소했으며 비GAAP 조정 EBITDA 손실은 370만 달러로 개선되었습니다. 회사는 분기 말에 5400만 달러의 현금 및 유가증권을 보유했고, 발행주식 수는 9억 799만 496,68주였습니다.

Zomedica (OTCQB:ZOMDF) a annoncé des résultats records pour le troisième trimestre de l'exercice clos au 30 septembre 2025, avec un chiffre d'affaires en hausse de 16% à 8,1 millions de dollars et une marge brute de 67%. Le chiffre d'affaires Diagnostics a augmenté de 51% et les nouveaux Services de Développement ont contribué à hauteur de 0,7 million de dollars durant ce trimestre. Les dépenses opérationnelles ont reculé de 0,5 million de dollars pour atteindre 12,0 millions, entraînant une perte nette inférieure de 6,1 millions et une perte EBITDA ajustée non GAAP améliorée de 3,7 millions. La société a terminé le trimestre avec 54,4 millions de dollars en espèces et valeurs mobilières et 979 949 668 actions en circulation.

Zomedica (OTCQB:ZOMDF) meldete Rekordergebnisse im dritten Quartal für den Zeitraum zum 30. September 2025, wobei der Umsatz um 16% auf 8,1 Mio. USD stieg und eine Bruttomarge von 67% erreicht wurde. Die Diagnostik-Umsätze stiegen um 51% und neue Development Services trugen in diesem Quartal 0,7 Mio. USD bei. Die Betriebskosten sanken sequenziell um 0,5 Mio. USD auf 12,0 Mio. USD, was zu einer geringeren Nettostloss von 6,1 Mio. USD und einer verbesserten Adjusted Non-GAAP EBITDA-Verlust von 3,7 Mio. USD führte. Das Unternehmen beendete das Quartal mit 54,4 Mio. USD in bar und Wertpapieren und 979.949.668 Aktien im Umlauf.

Zomedica (OTCQB:ZOMDF) أعلنت عن نتائج ربع ثالث قياسية للفترة المنتهية في 30 سبتمبر 2025، مع إيرادات ارتفعت بنسبة 16% إلى 8.1 مليون دولار وهامش إجمالي قدره 67%. ارتفعت إيرادات التشخيص بنسبة 51% وساهمت خدمات التطوير الجديدة بمقدار 0.7 مليون دولار في هذا الربع. انخفضت المصروفات التشغيلية بمقدار 0.5 مليون دولار على أساس فاصل ليصل الإجمالي إلى 12.0 مليون دولار، ما أدى إلى انخفاض صافي الخسارة إلى 6.1 مليون دولار وتحسن خسارة EBITDA المعدلة غير GAAP إلى 3.7 مليون دولار. أنهت الشركة الربع بوجود 54.4 مليون دولار من النقد والأوراق المالية و979,949,668 سهماً قائماً.

Positive
  • Revenue +16% to $8.1M
  • Diagnostics revenue +51% year-over-year
  • Gross margin at 67%
  • Liquidity of $54.4M
  • OPEX reduced by $0.5M (4%)
Negative
  • Net loss of $6.1M for Q3 2025
  • Operating expenses $12.0M exceed revenue
  • Large share count: 979,949,668 outstanding

Insights

Zomedica shows improving revenue, strong gross margins, reduced losses, and ample liquidity to fund near-term growth.

Zomedica grew quarterly revenue by 16% to $8.1 million and reported a 67% gross margin, driven by Therapeutic Device sales and 51% Diagnostics growth. The company added a new Development Services stream that contributed $0.7M and reported $54.4 million in cash and securities as of September 30, 2025, which supports ongoing operations while losses shrink.

Performance depends on continued adoption of the TRUFORMA platform, recurring consumable sales, and the new Development Services bookings; operating expenses fell $0.5 million quarter-over-quarter and net loss narrowed to $6.1 million. Key near-term items to watch are the filed Form 10-Q for additional detail, the company webinar on November 21, 2025, and whether Development Services revenue and international distribution agreements convert to repeatable revenue within the next several quarters.

Zomedica posts highest quarterly revenue ever and record year-over-year revenue for 19th straight quarter!

ANN ARBOR, MI / ACCESS Newswire / November 4, 2025 / Zomedica Corp. (OTCQB:ZOMDF) ("Zomedica" or the "Company"), an animal health company offering point-of-care diagnostic and therapeutic products for equine and companion animals, today reported consolidated financial results for the third quarter ended September 30, 2025.

"Delivering 16% growth and achieving record year-over-year revenue for the 19th straight quarter demonstrates the consistency and resilience of our business. Crossing $8 million in quarterly sales for the first time is a proud moment for our company and a clear indicator that our long-term strategy is working" said Larry Heaton, Chief Executive Officer of Zomedica.

"Fueled by robust demand for our PulseVet® and Assisi® therapeutic device products, continued accelerated growth and adoption of our diagnostic products, including our expanding TRUFORMA® platform, and the successful introduction of our new Development Services revenue stream, we delivered the strongest quarter in company history.

"As we continue to identify ways to leverage our infrastructure and intellectual property assets, the new Development Services business segment captures revenue we generate from providing development and engineering services along with contract manufacturing and licensing of our intellectual property. During the quarter, we booked $0.7M in revenue in this new segment, produced from our work on behalf of a company in the human health space. We are optimistic about our ability to continue to generate increasing revenue from this new segment, providing planned operating leverage.

"Ongoing portfolio expansion and optimization of our commercial organization continue to drive strong performance, as evidenced by 51% growth in our Diagnostic segment and 14% growth in total Consumable sales year-over-year. This performance reinforces our recurring revenue model and positions us for sustained long-term growth.

"International sales continue to grow, with sales up 16% compared to the third quarter of 2024, driven by a combination of organic growth and orders from new distributor partners. We are especially pleased with the success of recent initiatives to expand our reach and extend the use of our suite of products. During the third quarter, we entered into a strategic distribution agreement with Pioneer Veterinary Products Limited, one of the United Kingdom's most respected veterinary distributors, broadening access to Zomedica's innovative products across one of the world's most advanced veterinary markets. We also strengthened partnerships with Grovet b.v. in the Netherlands and UXR in Canada, further expanding our network and advancing our mission to deliver innovative diagnostic and therapeutic solutions for both practitioners and pet owners globally.

"We remain committed to continuously advancing our products to meet the evolving needs of veterinarians and their patients. In the third quarter, we expanded our TRUFORMA® diagnostic platform with the addition of feline testing for cobalamin and folate and secured four additional U.S. patents extending our TRUFORMA assay capabilities and protecting our TRUVIEW® microscope. We look forward to introducing further enhancements to our VETGuardian® system and launching our TRUVIEW AI platform in the coming quarter.

"Gross margin, a key component of reaching profitability, came in at 67%.

"Our disciplined execution of cost-reduction initiatives continues to pay off, resulting in a $0.5 million reduction in OPEX for the quarter ended September 30, 2025 and $2.5 million year-to-date. These efforts are driving greater efficiency across the organization, reducing cash burn, and positioning us for stronger, more sustainable growth.

"Building on the momentum we've achieved through the third quarter and supported by the strength of our balance sheet, we believe we are well positioned to execute on our strategy to accelerate the global adoption of our innovative portfolio, providing us with a clear line of sight to cash flow breakeven and profitability" concluded Mr. Heaton.

2025 Third Quarter Financial Highlights

Revenue for the third quarter of 2025 grew by 16% to $8.1 million, compared to third quarter 2024 revenue, highlighted by 51% growth in our Diagnostics segment, driven primarily by accelerating adoption of our TRUFORMA® point-of-care, diagnostic platform and the introduction of Development Services revenue.

Revenue by Product Segment:

  • Diagnostics segment revenue, comprised of our TRUFORMA, TRUVIEW®, and VETGuardian® products, was $0.7 million, up 51% over third quarter 2024 revenues, primarily driven by accelerating adoption of our TRUFORMA point-of-care, diagnostic platform and our expanded menu of assays.

  • Therapeutic Device segment revenue, comprised of our PulseVet® and Assisi® products, was $6.7 million, up 3% from third quarter 2024 revenues.

  • Development Services segment revenue, related to our continued pursuit of strategic opportunities and value capture within the human health sector, was $0.7M for the quarter.

Revenue by Product Category:

  • Consumable revenues grew to $5.4 million, up 14% over third quarter 2024 revenues, driven primarily by accelerating adoption of our TRUFORMA products and the continued, strong sales of PulseVet trodes, from both new device installations and reorders associated with existing systems. We anticipate that this growth will further compound and recur in future periods as more devices are installed.

  • Capital revenues, comprised of PulseVet and VETGuardian product sales, were $2.2 million.

  • Engineering Services revenues, associated with our Development Services segment, were $0.5M for the quarter.

Gross margin was 67% for the third quarter of 2025.

*Reported financial metrics, including year-over-year and sequential percentage changes, are calculated using actual results, which may not match calculations done using the figures shown in this press release due to rounding. Please refer to the Company's Form 10-Q for additional detail.

2025 Third Quarter Results Review

Revenue for the three months ended September 30, 2025, was $8.1 million, compared to $7.0 million for the three months ended September 30, 2024, an increase of $1.1 million or 16%.

Margins remained strong at 67%.

Total operating expenses were $12.0 million, compared to $12.5 million for the three months ended September 30, 2024, a decrease of $0.5 million or 4%.

Research and development expenses were $1.8 million, slightly down from research and development expenses for the three months ended September 30, 2024. Costs in this area are related to the continued buildup of internal capabilities to develop, test, and manufacture our next generation of therapeutic and diagnostic products.

Selling and marketing expenses were $4.3 million, compared to $3.9 million for the three months ended September 30, 2025, an increase of $0.4 million or 12%, primarily driven by the increased headcount of our sales department relative to the prior year, as well as higher commissions associated with sales growth.

General and administrative expenses were $5.9 million, compared to $6.8 million for the three months ended September 30, 2024, a decrease of $0.9 million or 13%.

Net loss for the three months ended September 30, 2025 was down 9% to $6.1 million, compared to $6.7 million for the three months ended September 30, 2024.

*Non-GAAP EBITDA loss (which includes adjustments for stock compensation) for the three months ended September 30, 2025, was down 19% to $3.9 million compared to an adjusted loss of $4.8 million for the three months ended September 30, 2024.

When adjusting for the non-recurring items noted above and other non-cash items, **Adjusted Non-GAAP EBITDA loss was down 14% to $3.7 million, compared to **Adjusted Non-GAAP EBITDA loss of $4.3 million for the third quarter of 2024.

Liquidity and Outstanding Share Capital

Zomedica had cash, cash equivalents, and available-for-sale securities of $54.4 million as of September 30, 2025.

As of September 30, 2025, Zomedica had 979,949,668 common shares issued and outstanding.

For complete financial results, please see Zomedica's filings on EDGAR and SEDAR+ or visit the Zomedica website at www.zomedica.com.

For percentage calculations please refer to the financial statements filed with the SEC on Tuesday, November 4, 2025, along with other public filings.

Zomedica's Fourth Friday at Four Webinar:

Zomedica Corp. is pleased to announce the next installment of its Fourth Friday at Four Webinar series, scheduled this month on the third Friday due to the Thanksgiving holiday, on Friday, November 21, 2025 at 4:00 PM ET, during which we will also review and discuss our third quarter financial performance.

For more information visit www.zomedica.com.

About Zomedica

Zomedica is a leading equine and companion animal healthcare company dedicated to improving animal health by providing veterinarians innovative therapeutic and diagnostic solutions. Our gold standard PulseVet® shock wave system, which accelerates healing in musculoskeletal conditions, has transformed veterinary therapeutics. Our suite of products also includes the Assisi Loop® line of therapeutic devices, along with the TRUFORMA® diagnostic platform, TRUVIEW® digital cytology system, VETGuardian® no-touch monitoring system, and VETIGEL® hemostatic gel, all designed to empower veterinarians to provide top-tier care. In the aggregate, their total addressable market in the U.S. exceeds $2 billion. Headquartered in Michigan, Zomedica employs approximately 150 people and manufactures and distributes its products from its world-class facilities in Georgia and Minnesota. Zomedica grew revenue 8% in 2024 to $27 million and maintains a strong balance sheet with approximately $54 million in liquidity as of September 30, 2025. Zomedica is advancing its product offerings, leveraging strategic acquisitions, and expanding internationally as we work to enhance the quality of care for pets, increase pet parent satisfaction, and improve the workflow, cash flow and profitability of veterinary practices. For more information visit www.zomedica.com.

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Cautionary Note Regarding Forward-Looking Statements

Except for statements of historical fact, this news release contains certain "forward-looking information" or "forward-looking statements" (collectively, "forward-looking information") within the meaning of applicable securities law. Forward-looking information is frequently characterized by words such as "plan", "expect", "project", "intend", "believe", "anticipate", "estimate" and other similar words, or statements that certain events or conditions "may" or "will" occur and include statements relating to our expectations regarding future results. Although we believe that the expectations reflected in the forward-looking information are reasonable, there can be no assurance that such expectations will prove to be correct. We cannot guarantee future results, performance, or achievements. Consequently, there is no representation that the actual results achieved will be the same, in whole or in part, as those set out in the forward-looking information.

Forward-looking information is based on the opinions and estimates of management at the date the statements are made, including assumptions with respect to economic growth, demand for the Company's products, the Company's ability to produce and sell its products, sufficiency of our budgeted capital and operating expenditures, the satisfaction by our strategic partners of their obligations under our commercial agreements and our ability to realize upon our business plans and cost control efforts.

Our forward-looking information is subject to a variety of risks and uncertainties and other factors that could cause actual events or results to differ materially from those anticipated in the forward-looking information. Some of the risks and other factors that could cause the results to differ materially from those expressed in the forward-looking information include, but are not limited to: uncertainty as to whether the human health company will enter into a written agreement for development and engineering services, contract manufacturing and/or licensing of our IP; uncertainty as to whether the new Development Services business segment will continue to generate revenue; the outcome of clinical studies; the application of generally accepted accounting principles, which are highly complex and involve many subjective assumptions, estimates, and judgments; uncertainty as to whether our strategies and business plans will yield the expected benefits; uncertainty as to the timing and results of development work and verification and validation studies; uncertainty as to the timing and results of commercialization efforts, including international efforts, as well as the cost of commercialization efforts, including the cost to develop an internal sales force and manage our growth; uncertainty as to our ability to realize the anticipated growth opportunities from our acquisitions; uncertainty as to our ability to supply products in response to customer demand; supply chain risks associated with tariff changes; uncertainty as to the likelihood and timing of any required regulatory approvals, and the availability and cost of capital; the ability to identify and develop and achieve commercial success for new products and technologies; veterinary acceptance of our products and purchase of consumables following adoption of our capital equipment; competition from related products; the level of expenditures necessary to maintain and improve the quality of products and services; changes in technology and changes in laws and regulations; our ability to secure and maintain strategic relationships; performance by our strategic partners of their obligations under our commercial agreements, including product manufacturing obligations; risks pertaining to permits and licensing, intellectual property infringement risks, risks relating to any required clinical trials and regulatory approvals, risks relating to the safety and efficacy of our products, the use of our products, intellectual property protection, and the other risk factors disclosed in our filings with the SEC and under our profile on SEDAR+ at www.sedarplus.com. Readers are cautioned that this list of risk factors should not be construed as exhaustive.

The forward-looking information contained in this news release is expressly qualified by this cautionary statement. We undertake no duty to update any of the forward-looking information to conform such information to actual results or to changes in our expectations except as otherwise required by applicable securities legislation. Readers are cautioned not to place undue reliance on forward-looking information.

Investor Relations Contact:

Zomedica Investor Relations
investors@zomedica.com
1-734-369-2555

Non-GAAP Measures

Non-GAAP EBITDA, Adjusted Non-GAAP EBITDA, and other measures presented on an adjusted basis are not recognized terms under U.S. GAAP and do not purport to be alternatives to the most comparable U.S. GAAP amounts. Since all companies do not use identical calculations, our definition and presentation of these measures may not be comparable to similarly titled measures reported by other companies. Management uses the identified non-GAAP measures to evaluate the operating performance of the Company and its business segments and to forecast future periods. Management believes these non-GAAP measures assist investors and other interested parties in evaluating Zomedica's on-going operations and provide important supplemental information to management and investors regarding financial and business trends relating to Zomedica's financial condition and results of operations. Investors should not consider these non-GAAP measures as alternatives to the related GAAP measures. Reconciliations of non-GAAP measures to their closest U.S. GAAP equivalent are presented below.

* Non-GAAP EBITDA is defined as net loss and comprehensive loss excluding amortization, depreciation, non-cash stock compensation, and taxes while reversing out the benefits derived from net interest income.

** Non-GAAP Adjusted EBITDA is defined as Non-GAAP EBITDA, as defined above, excluding impairment charges and non-recurring items; including but not limited to specialized accounting, tax, and audit services, new facility integration / start-up costs, and other one-time items.

ZOMEDICA CORP.
RECONCILIATION OF NON-GAAP FINANCIAL MEASURES
(amounts in thousands)
(unaudited)

Three Months Ended September 30,

2025

2024

Net loss and comprehensive loss

$

(6,105

)

$

(6,333

)

Amortization expense

1,395

1,611

Depreciation expense

506

417

Stock-compensation expense

868

473

Interest income

(561

)

(977

)

Income tax benefit

(19

)

(27

)

Non-GAAP EBITDA loss

$

(3,916

)

$

(4,836

)


Impairment expense

-

-

Proforma adjustments (1)

214

523

Adjusted Non-GAAP EBITDA loss

$

(3,702

)

$

(4,313

)

(1)

Proforma adjustments for the three months ended September 30, 2025 included $73 of one-time general and administrative expenses, $97 of one-time research and development expenses, $5 of one-time selling and marketing expenses, and $39 of non-recurring losses on disposals of assets

ZOMEDICA CORP.
RECONCILIATION OF NON-GAAP FINANCIAL MEASURES
(amounts in thousands)
(unaudited)

Nine Months Ended September 30,

2025

2024

Net loss and comprehensive loss

$

(77,223

)

$

(39,536

)

Amortization expense

4,499

4,834

Depreciation expense

1,535

1,102

Stock-compensation expense

1,746

2,432

Interest income

(1,920

)

(3,108

)

Income tax benefit

(64

)

(336

)

Non-GAAP EBITDA loss

$

(71,427

)

$

(34,612

)


Impairment expense

55,833

16,024

Proforma adjustments (1)

625

3,798

Adjusted Non-GAAP EBITDA loss

$

(14,969

)

$

(14,790

)

(1)

Proforma adjustments for the three months ended September 30, 2025 included $480 of one-time general and administrative expenses, $97 of one-time research and development expenses, $9 of one-time selling and marketing expenses, and $39 of non-recurring losses on disposals of assets

SOURCE: Zomedica Corp.



View the original press release on ACCESS Newswire

FAQ

What were Zomedica (ZOMDF) revenues and gross margin in Q3 2025?

Zomedica reported $8.1M in revenue for Q3 2025 with a 67% gross margin.

How did Zomedica's Diagnostics segment perform in Q3 2025 (ZOMDF)?

Diagnostics revenue increased 51% year-over-year, driven by TRUFORMA adoption.

What was Zomedica's net loss and adjusted EBITDA loss in Q3 2025?

Net loss was $6.1M; Adjusted Non-GAAP EBITDA loss improved to $3.7M.

How much cash and securities did Zomedica (ZOMDF) have at September 30, 2025?

Zomedica reported $54.4M in cash, cash equivalents, and available-for-sale securities.

Did Zomedica launch any new revenue streams in Q3 2025 (ZOMDF)?

Yes — the company recorded $0.7M in Development Services revenue during Q3 2025.

How did Zomedica's operating expenses change in Q3 2025 versus Q3 2024?

Total operating expenses declined by $0.5M (about 4%) to $12.0M in Q3 2025.

When will Zomedica (ZOMDF) host its next Fourth Friday at Four webinar to discuss Q3 2025?

The webinar is scheduled for Friday, November 21, 2025 at 4:00 PM ET.
Zomedica Corp

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