Medical Device Manufacturer · US , Los Angeles , CA

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

2 submissions · 2 cleared · Since 2023

Total

Cleared

Denied

Therabody, Inc. has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Latest FDA clearance: Aug 2024. Active since 2023. Primary specialty: General & Plastic Surgery.

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

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

2 devices

1-2 of 2