Marlo Surgical Technology

Marlo Surgical Technology — FDA 510(k) Submissions

Marlo Surgical Technology has submitted 28 FDA 510(k) premarket notifications since 1985, of which 28 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, Gynecologic (and Accessories), Laparoscope, General & Plastic Surgery, Cannula, Intrauterine Insemination, Instrument, Surgical, Disposable, Tenaculum, Uterine . Use the specialty filter in the sidebar to narrow results.