Bodycad Laboratories, Inc.

Bodycad Laboratories, Inc. — FDA 510(k) Submissions

Bodycad Laboratories, Inc. has submitted 16 FDA 510(k) premarket notifications since 2017, of which 16 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer, Plate, Fixation, Bone, Orthopaedic Surgical Planning And Instrument Guides . Use the specialty filter in the sidebar to narrow results.