J. Jamner Surgical Instruments, Inc.

J. Jamner Surgical Instruments, Inc. — FDA 510(k) Submissions

J. Jamner Surgical Instruments, Inc. has submitted 11 FDA 510(k) premarket notifications since 1977, of which 11 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, General & Plastic Surgery, Electrosurgical, Cutting & Coagulation & Accessories, Nasopharyngoscope (flexible Or Rigid), Coagulator-cutter, Endoscopic, Unipolar (and Accessories), Tenaculum, Uterine . Use the specialty filter in the sidebar to narrow results.