Embody, Inc. - FDA 510(k) Cleared Devices
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.
FDA 510(k) cleared devices by Embody, Inc.
6 devices
Cleared
Sep 19, 2025
Tapestry Biointegrative Implant
Orthopedic
29d
Cleared
Jun 02, 2023
ACTIVBRAID™
General & Plastic Surgery
163d
Cleared
May 23, 2022
Tapestry Biointegrative Implant
Orthopedic
59d
Cleared
Apr 08, 2022
Bioabsorbable Anchor
Orthopedic
112d
Cleared
Nov 02, 2021
Tapestry Biointegrative Implant
Orthopedic
102d
Cleared
Oct 19, 2020
TAPESTRY Biointegrative Implant
Orthopedic
130d