Origin Medsystems, Inc.

Origin Medsystems, Inc. — FDA 510(k) Submissions

Origin Medsystems, Inc. has submitted 50 FDA 510(k) premarket notifications since 1989, of which 49 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, General & Plastic Surgery, Laparoscope, Gynecologic (and Accessories), Pneumoperitoneum Needle, System, Cement Removal Extraction, Cannula, Surgical, General & Plastic Surgery . Use the specialty filter in the sidebar to narrow results.