Medical Device Manufacturer · US , Redmond , WA

Gynex Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1998

Total

Cleared

Denied

Gynex Corp. has 5 FDA 510(k) cleared medical devices. Based in Redmond, US.

Historical record: 5 cleared submissions from 1998 to 2006. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Gynex Corp. Filter by specialty or product code using the sidebar.

Gynex Corp. is one of 7362 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Gynex Corp.

5 devices

1-5 of 5