Perimeter Medical Imaging AI’s ‘Claire’ Becomes First FDA-approved AI-Enabled Imaging Device for Breast Cancer Surgery

TORONTO and DALLAS, March 3, 2026 /PRNewswire/ - Perimeter Medical Imaging AI, Inc. (TSXV: PINK) (OTCQX: PYNKF) ("Perimeter" or the "Company"), a commercial-stage medical technology company, announced today that it has received U.S. Food and Drug Administration ("FDA") premarket approval ("PMA") for Claire™ (formerly the Perimeter OCT B-Series with ImgAssist AI 2.0), the first AI-enabled imaging device approved in the United States for intraoperative breast cancer margin assessment.

“Repeat breast cancer surgeries due to residual disease remain a significant clinical, health, and economic burden,” said Perimeter CEO, Adrian Mendes. “Claire’s FDA approval marks a major milestone in breast cancer care, as we advance our goal of reducing repeat surgeries so that no patient has to be told ‘we didn’t get it all.’ We plan to begin a nationwide launch in the coming weeks so that surgeons can rapidly adopt the industry’s first FDA-approved real-time AI-powered imaging technology for breast cancer surgery.”

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