Aerin Medical, Inc.

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

Aerin Medical, Inc. has submitted 9 FDA 510(k) premarket notifications since 2015, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Needle, Conduction, Anesthetic (w/wo Introducer) . Use the specialty filter in the sidebar to narrow results.