Medical Device Manufacturer · US , Lake Forest , CA

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

2 submissions · 2 cleared · Since 2025

Total

Cleared

Denied

Biodynamik, Inc. has 2 FDA 510(k) cleared medical devices. Based in Lake Forest, US.

Latest FDA clearance: Feb 2026. Active since 2025. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Biodynamik, Inc.

2 devices

1-2 of 2