Eder Instrument Co, Inc.

Eder Instrument Co, Inc. — FDA 510(k) Submissions

Eder Instrument Co, Inc. has submitted 10 FDA 510(k) premarket notifications since 1979, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, Gynecologic (and Accessories), Forceps, General & Plastic Surgery, Probe, Endoscopic Video Imaging System/component, Gastroenterology-urology, Bronchoscope (flexible Or Rigid) . Use the specialty filter in the sidebar to narrow results.