Acera Surgical, Inc. - FDA 510(k) Cleared Devices

Acera Surgical, Inc. has 7 FDA 510(k) cleared medical devices. Based in St. Louis, US.

Latest FDA clearance: Jun 2025. Active since 2016. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Secure Biomed Evalutations as regulatory consultant.