Medical Device Manufacturer · US , St. Louis , MO

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

7 submissions · 7 cleared · Since 2016

Total

Cleared

Denied

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.

FDA 510(k) cleared devices by Acera Surgical, Inc.

7 devices

1-7 of 7