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.

Stryker Trauma GmbH 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 - Stryker Trauma GmbH

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: May 28, 2026