Embody, Inc.

Embody, Inc. — FDA 510(k) Submissions

Embody, Inc. has submitted 6 FDA 510(k) premarket notifications since 2020, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon, Fastener, Fixation, Biodegradable, Soft Tissue, Suture, Nonabsorbable, Synthetic, Polyethylene . Use the specialty filter in the sidebar to narrow results.