Medical Device Manufacturer · US , San Antonio , TX

Teftec Corp. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1996

Total

Cleared

Denied

Teftec Corp. has 8 FDA 510(k) cleared medical devices. Based in San Antonio, US.

Historical record: 8 cleared submissions from 1996 to 2002. Primary specialty: Physical Medicine.

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

Teftec 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 - Teftec Corp.

8 devices

1-8 of 8