Alafair Biosciences, Inc.

Alafair Biosciences, Inc. — FDA 510(k) Submissions

Alafair Biosciences, Inc. has submitted 7 FDA 510(k) premarket notifications since 2016, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mesh, Surgical, Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon, Cuff, Nerve . Use the specialty filter in the sidebar to narrow results.