Medical Device Manufacturer · US , Kennesaw , GA

Dornier - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1999

Total

Cleared

Denied

Dornier has 3 FDA 510(k) cleared medical devices. Based in Kennesaw, US.

Historical record: 3 cleared submissions from 1999 to 2001. Primary specialty: Gastroenterology & Urology.

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

Dornier 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 - Dornier

3 devices

1-3 of 3