Gynex Corp.

Gynex Corp. — FDA 510(k) Submissions

Gynex Corp. has submitted 5 FDA 510(k) premarket notifications since 1998, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tenaculum, Uterine, Electrocautery, Gynecologic (and Accessories), Colposcope (and Colpomicroscope), Instrument, Manual, Specialized Obstetric-gynecologic, Set, Anesthesia, Paracervical . Use the specialty filter in the sidebar to narrow results.