Medical Device Manufacturer · US , Los Angeles , CA

U.S. Dentek Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1988

Total

Cleared

Denied

U.S. Dentek Corp. has 4 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 4 cleared submissions from 1988 to 1996. Primary specialty: Dental.

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

U.S. Dentek 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 - U.S. Dentek Corp.

4 devices

1-4 of 4