Medical Device Manufacturer · DE , Rostock

Artoss GmbH - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2015

Total

Cleared

Denied

Artoss GmbH has 3 FDA 510(k) cleared medical devices. Based in Rostock, DE.

Historical record: 3 cleared submissions from 2015 to 2019. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Artoss GmbH

3 devices

1-3 of 3