Medical Device Manufacturer · CA , Quebec City

Bodycad Laboratories, Inc. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 2017
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.

510(k) submissions have been managed by BioVera, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Bodycad Laboratories, Inc.
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