Resilia, Inc. - FDA 510(k) Cleared Devices

Resilia, Inc. has 1 FDA 510(k) cleared medical devices. Based in Moncton, CA.

Latest FDA clearance: Apr 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Resilia, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by QUARAS, LLC as regulatory consultant.