Medical Device Manufacturer · DE , Dieburg

Osartis GmbH

6 submissions · 6 cleared · Since 2019

Total

Cleared

Denied

Osartis GmbH has 6 FDA 510(k) cleared medical devices. Based in Dieburg, DE.

Latest FDA clearance: Nov 2024. Active since 2019. Primary specialty: Orthopedic.

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

6 devices

1–6 of 6

Data Source

FDA 510(k) public files . 174,402 total devices indexed.