Solos Endoscopy, Inc.

Solos Endoscopy, Inc. — FDA 510(k) Submissions

Solos Endoscopy, Inc. has submitted 21 FDA 510(k) premarket notifications since 1990, of which 21 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cannula And Trocar, Suprapubic, Non-disposable, Electrosurgical, Cutting & Coagulation & Accessories, Forceps, General & Plastic Surgery, Scissors, General, Surgical, Carrier, Ligature . Use the specialty filter in the sidebar to narrow results.