Theramicro

Theramicro — FDA 510(k) Submissions

Theramicro has submitted 2 FDA 510(k) premarket notifications since 2025, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mesh, Surgical, Non-resorbable, Orthopedics, Reinforcement Of Ligament, Fastener, Fixation, Nondegradable, Soft Tissue . Use the specialty filter in the sidebar to narrow results.