Medical Device Manufacturer · US , Elk Grove Village , IL

Teledyne Getz - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1990

Total

Cleared

Denied

Teledyne Getz has 5 FDA 510(k) cleared medical devices. Based in Elk Grove Village, US.

Historical record: 5 cleared submissions from 1990 to 1992. Primary specialty: Dental.

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

Teledyne Getz 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 - Teledyne Getz

5 devices

1-5 of 5