Medical Device Manufacturer · US , Walker , MI

Endotek Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1980

Total

Cleared

Denied

Endotek Corp. has 2 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 2 cleared submissions from 1980 to 1984. Primary specialty: Gastroenterology & Urology.

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

Endotek Corp. 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 - Endotek Corp.

2 devices

1-2 of 2