Endo Technic Corp.

Endo Technic Corp. — FDA 510(k) Submissions

Endo Technic Corp. has submitted 10 FDA 510(k) premarket notifications since 1986, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, Gynecologic (and Accessories), Powered Laser Surgical Instrument, Laparoscope, General & Plastic Surgery, Coagulator, Culdoscopic (and Accessories), System, Dental, Hydrokinetic, Caries Removal & Cavity Preparation . Use the specialty filter in the sidebar to narrow results.