Medical Device Manufacturer · US , Mahwah , NJ

Stryker Trauma GmbH - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2015

Total

Cleared

Denied

Stryker Trauma GmbH has 7 FDA 510(k) cleared medical devices. Based in Mahwah, US.

Historical record: 7 cleared submissions from 2015 to 2020. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Stryker Trauma GmbH

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 4,872 total devices indexed.

Last updated: Mar 22, 2026