Medical Device Manufacturer · US , Irvine , CA

Endomedix - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1992

Total

Cleared

Denied

Endomedix has 7 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 7 cleared submissions from 1992 to 1994. Primary specialty: Gastroenterology & Urology.

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

Endomedix is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Endomedix

7 devices

1-7 of 7