Perimeter Announces Preliminary Unaudited Fourth Quarter and Full Year 2025 Financial Results Marked by Record Revenues and Improved Operating Performance
Conference Call/Webcast Today at
"2025 marked a pivotal inflection point for Perimeter as we executed against our strategic roadmap and positioned the Company for what we believe is a significant long-term growth opportunity," commented
"Building on this strong foundation, we are now squarely focused on the upcoming commercial launch of Claire OCT and on expanding our presence with leading healthcare institutions across
Business Highlights
First FDA 510(k)-Cleared Device: Perimeter S-Series OCT
- While the
U.S. Food and Drug Administration ("FDA") continued to review the Company's Premarket Approval ("PMA") application for its next-generation system for use during breast-conserving surgeries inthe United States , commercial market traction with the Company's first FDA-cleared product under a general indication, the Perimeter S-Series OCT system, continued to grow:- Q4-2025 revenue of
$711,000 , up 143% year-over-year compared to Q4-2024, and up 33% sequentially from Q3-2025. - Full year 2025 revenue of
$2.3 million was 172% higher than revenue for 2024. - In
November 2025 , Dr.Kayla Griffith , Breast Surgical Oncologist, and HCA HealthONE Rose, part of theHCA HealthONE network of 9 hospitals and 17 surgery centers in theRocky Mountain region and one of the largest health systems in theDenver area, were the first inColorado to adopt the Company's S-Series OCT for tissue visualization in the operating room. - In
January 2026 , Perimeter entered into an agreement withIntermountain Health , the largest nonprofit healthcare system in theIntermountain West region, to enable the deployment of S-Series OCT for tissue visualization in the operating rooms atIntermountain Health LDS Hospital inSalt Lake City andIntermountain Health American Fork Hospital inAmerican Fork, Utah .
- Q4-2025 revenue of
Introducing Claire™, the First AI-enabled Imaging Device to Receive FDA PMA Approval for Intraoperative Breast Cancer Margin Assessment
- In early
March 2026 , Claire, which combines Perimeter's proprietary artificial intelligence ("AI") with its patented wide-field OCT imaging to enable high-resolution, real-time evaluation of excised tumor margins, received FDA PMA approval. - Claire delivers 10 times higher resolution than standard X-ray and ultrasound at 2mm imaging depth - the clinically relevant margin width for breast cancer margin assessment. Claire's innovative AI technology was trained on Perimeter's proprietary and growing OCT image library of over 2 million breast tissue images.
- The technology, which previously received Breakthrough Device designation from the FDA, is designed to enhance surgeons' ability to detect difficult-to-see cancer during breast-conserving surgery and potentially reduce the need for re-operations.
- Perimeter is making final preparations for the
U.S. commercial launch of Claire, which it expects to begin in Q2-2026.
Corporate
- In
December 2025 , Perimeter announced the closing of a non-brokered private placement where the Company issued an aggregate of 19,757,306 Units at a price ofC$0.18 per Unit for aggregate gross proceeds ofC$3,556,315 . - In
February 2026 , Perimeter entered into cancellation agreements with certain employees and consultants of the Company, pursuant to which it cancelled 2,175,619 previously issued stock options (the "Original Options"), exercisable at prices ranging fromC$0.38 toC$2.85 , and replaced the same number of Original Options with new stock options, exercisable at a price ofC$0.30 per common share. No directors or officers of the Company have entered or will enter into cancellation agreements, have had Original Options cancelled or received Replacement Options. - In
March 2026 , Perimeter entered into a warrant cancellation agreement withSC Master Holdings LLC ("Social Capital "), pursuant to whichSocial Capital agreed to surrender 14,466,667 common share purchase warrants of the Company for cancellation, for no consideration.
Summary Preliminary Unaudited Fourth Quarter 2025 Financial Results 1
Revenue was approximately
Operating expenses for the three months ended
Fourth quarter 2025 net loss was approximately
Summary Preliminary Unaudited Full Year 2025 Financial Results 1
For the year ended
Perimeter's full year 2025 operating expenses were approximately
Full year 2025 net loss was approximately
Cash used in operating activities in the 12 months ended
As of
Perimeter currently anticipates that it will file its annual audited consolidated financial statements, its annual management's discussion and analysis, and its certification of annual filings for the year ended
1 Preliminary and unaudited financial results are subject to customary financial statement procedures by the Company and its auditors. Actual results could be affected by subsequent events or determinations. While the Company believes there is a reasonable basis for these preliminary financial results, the results involve known and unknown risks and uncertainties that may cause actual results to differ materially. Preliminary fiscal results represent forward-looking information. See "Cautionary Note Regarding Forward-Looking Information and Statements" and "Financial Outlook". The audit of the consolidated financial statements for the year and three months ended
Conference Call
The Company will host a conference call and live audio webcast today at
About
Based in
Indications for Use: The Claire OCT System is an adjunctive three-dimensional imaging tool which provides volumetric cross-sectional, real-time depth visualization, coupled with an artificial intelligence computer-aided detection algorithm which identifies and marks focal areas suspicious for breast cancer. It is used concurrently with physician interpretation of the images. The Claire OCT System is intended for use in conjunction with other standard methods for evaluation of the margins of excised lumpectomy tissue during surgical procedures in patients with a biopsy-confirmed diagnosis of breast cancer.
The Claire OCT System should not be used to replace standard tissue histopathology assessment and should not be used for diagnosis. The device is not intended for use in any of the following individuals: under the age of 18, male, have metastatic cancer (Stage IV), have lobular carcinoma as their primary diagnosis, have had previous ipsilateral breast surgery for benign or malignant disease within two years (including implants and breast augmentation), patients with multi-centric disease (histologically diagnosed cancer in two different quadrants of the breast), unless resected in a single specimen, patients with bilateral disease (diagnosed cancer in both breasts), patients who are currently lactating, patients who are currently pregnant, or concurrent use in surgeries with cryo-assisted localization. Refer to prescriber labeling for full safety information.
Neither the
Forward-Looking Statements
This news release contains statements that constitute "forward-looking information" within the meaning of applicable Canadian securities legislation. In this news release, words such as "may," "would," "could," "will," "likely," "believe," "expect," "anticipate," "intend," "plan," "estimate," and similar words and the negative form thereof are used to identify forward-looking statements. Forward-looking information may relate to management's future outlook and anticipated events or results and may include statements or information regarding the Company's results for the three and 12 months ended
Financial Outlook
This press release contains a financial outlook within the meaning of applicable Canadian securities laws. The financial outlook has been prepared by management of the Company to provide an outlook for certain of the Company's financial results for the three and 12 months ended
Contacts
Investor Relations
Direct: 647-872-4849
Email: skilmer@perimetermed.com
Chief Executive Officer
Toll-free: 888-988-7465 (PINK)
Email: investors@perimetermed.com
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