Perimeter Medical Imaging to Announce Topline Results from Pivotal Clinical Trial Evaluating B-Series OCT with ImgAssist AI in Breast-Conserving Surgeries on November 20th; Conference Call to Follow

TORONTO and DALLAS, Nov. 18, 2024 /PRNewswire/ – Perimeter Medical (TASE:) Imaging AI, Inc. (TSXV:  PINK) (OTC:  PYNKF) (“Perimeter” or the “Company”), a commercial-stage medical technology company, announced that it will report topline results from the pivotal study evaluating the use of its next-generation Perimeter B-Series OCT system, which combines proprietary artificial intelligence (“AI”) technology with optical coherence tomography (“OCT”), during breast-conserving surgeries after market close on Wednesday, November 20, 2024. Following the announcement, Perimeter management will host a webcast and conference call to discuss the topline results.

Perimeter B-Series OCT with ImgAssist AI Pivotal Trial Topline Results Conference Call Details:

The call will also be broadcast live and archived on the Company’s website under “News/Events” in the Investors section.

About Perimeter Medical Imaging AI, Inc.

Based in Toronto, Canada and Dallas, Texas, Perimeter Medical Imaging AI (TSXV: PINK) (OTC: PYNKF) is a medical technology company driven to transform cancer surgery with ultra-high-resolution, real-time, advanced imaging tools to address areas of high unmet medical need. Available across the U.S., our FDA-cleared Perimeter S-Series OCT system provides real-time, cross-sectional visualization of excised tissues at the cellular level. The breakthrough-device-designated investigational Perimeter B-Series OCT with ImgAssist AI represents our next-generation artificial intelligence technology that is currently being evaluated in a pivotal clinical trial, with support from a grant of up to US$7.4 million awarded by the Cancer Prevention and Research Institute of Texas. The company’s ticker symbol “PINK” is a reference to the pink ribbons used during Breast Cancer Awareness Month.

Perimeter B-Series OCT is limited by U.S. law to investigational use and not available for sale in the United States. Perimeter S-Series OCT has 510(k) clearance under a general indication and has not been evaluated by the U.S. FDA specifically for use in breast tissue, breast cancer, other types of cancer, margin evaluation, and reducing re-excision rates. The safety and effectiveness of these uses has not been established. For more information, please visit www.perimetermed.com/disclosures.

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