Medical Device Manufacturer · US , Potomac , MD

Friatec AG - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1998

Recent clearances: FRIALIT-2 AUROBASE MODEL NUMBERS 45-2446, 45-2456, 45-2466, 45-2476, FRIALIT-2 CORABASE, FRIOS BONESHIELD

Official Website

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Friatec AG Dental ✕

6 devices

1-6 of 6

Cleared Oct 22, 1998

FRIALIT-2 AUROBASE MODEL NUMBERS 45-2446, 45-2456, 45-2466, 45-2476

Cleared Sep 04, 1998

FRIALIT-2 CORABASE

Cleared May 07, 1998

FRIOS BONESHIELD

Cleared Mar 11, 1998

FRIALIT-2 PROTECT ABUTMENT

Cleared Feb 10, 1998

FRIALIT -2 SCREW

Cleared Feb 10, 1998

FRIALIT-2 CYLINDER

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Sep 08, 2026