Medical Device Manufacturer · US , Golden , CO

Unisensor AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2001

Total

Cleared

Denied

Unisensor AG has 2 FDA 510(k) cleared medical devices. Based in Golden, US.

Historical record: 2 cleared submissions from 2001 to 2007. Primary specialty: Gastroenterology & Urology.

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

Unisensor 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 - Unisensor AG

2 devices

1-2 of 2