Surgical Technology Laboratories, Inc.

Surgical Technology Laboratories, Inc. — FDA 510(k) Submissions

Surgical Technology Laboratories, Inc. has submitted 12 FDA 510(k) premarket notifications since 1980, of which 12 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implant, Malar, Prosthesis, Chin, Internal, Prosthesis, Nose, Internal, Forceps, General & Plastic Surgery, Airway, Oropharyngeal, Anesthesiology . Use the specialty filter in the sidebar to narrow results.