Medical Device Manufacturer · US , Potomac , MD

Friatec AG - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1998

Total

Cleared

Denied

Friatec AG has 6 FDA 510(k) cleared medical devices. Based in Potomac, US.

Historical record: 6 cleared submissions from 1998 to 1998. Primary specialty: Dental.

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

Friatec AG 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 - Friatec AG

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026