Miromatrix Medical, Inc.

Miromatrix Medical, Inc. — FDA 510(k) Submissions

Miromatrix Medical, Inc. has submitted 6 FDA 510(k) premarket notifications since 2014, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mesh, Surgical, Wound Dressing With Animal-derived Material(s), Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery . Use the specialty filter in the sidebar to narrow results.