Aevumed, Inc.

Aevumed, Inc. — FDA 510(k) Submissions

Aevumed, Inc. has submitted 7 FDA 510(k) premarket notifications since 2018, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Fastener, Fixation, Nondegradable, Soft Tissue . Use the specialty filter in the sidebar to narrow results.