Medical Device Manufacturer · US , Norfolk , VA

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

6 submissions · 6 cleared · Since 2020

Recent clearances: Tapestry Biointegrative Implant, ACTIVBRAID™, Tapestry Biointegrative Implant

6
Total
6
Cleared
0
Denied

Embody, Inc. has 6 FDA 510(k) cleared medical devices. Based in Norfolk, US.

Latest FDA clearance: Sep 2025. Active since 2020. Primary specialty: Orthopedic.

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

510(k) submissions have been managed by Bruder Consulting and Venture Group as regulatory consultant.

FDA 510(k) Regulatory Record - Embody, Inc.

6 devices
1-6 of 6
Filters