Aesthetic and Reconstructive Technologies, Inc.

Aesthetic and Reconstructive Technologies, Inc. — FDA 510(k) Submissions

Aesthetic and Reconstructive Technologies, Inc. has submitted 10 FDA 510(k) premarket notifications since 2002, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Elastomer, Silicone Block, Implant, Muscle, Pectoralis, Prosthesis, Chin, Internal, Prosthesis, Nose, Internal, Implant, Malar . Use the specialty filter in the sidebar to narrow results.