Bodycad Laboratories, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Bodycad Laboratories, Inc. has 16 FDA 510(k) cleared orthopedic devices. Based in Quebec City, CA.
Latest FDA clearance: Oct 2025. Active since 2017.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bodycad Laboratories, Inc.
16 devices
Cleared
Oct 28, 2025
Fine Osteotomy™
Orthopedic
29d
Cleared
Oct 21, 2025
Fine TTO™
Orthopedic
251d
Cleared
Aug 21, 2025
Fine Osteotomy™
Orthopedic
147d
Cleared
Sep 05, 2024
Fine Osteotomy™
Orthopedic
114d
Cleared
Apr 12, 2024
Fine Osteotomy™
Orthopedic
29d
Cleared
Feb 09, 2024
Fine Osteotomy™
Orthopedic
31d
Cleared
Jun 02, 2023
Fine Osteotomy™
Orthopedic
28d
Cleared
Oct 12, 2021
BC Reflex Uni Knee System
Orthopedic
81d
Cleared
Aug 20, 2021
BC Reflex Uni Knee System
Orthopedic
60d
Cleared
Jul 28, 2021
FINE Osteotomy
Orthopedic
61d
Cleared
Mar 12, 2021
BC Reflex Uni Knee System
Orthopedic
84d
Cleared
Mar 25, 2020
FINE Osteotomy around the knee
Orthopedic
90d