Medical Device Manufacturer · DE , Freiburg, Baden-Wuerttemberg

Stryker Corporate - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2013

Total

Cleared

Denied

Stryker Corporate has 6 FDA 510(k) cleared medical devices. Based in Freiburg, Baden-Wuerttemberg, DE.

Historical record: 6 cleared submissions from 2013 to 2016. Primary specialty: Orthopedic.

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

510(k) submissions have been managed by Stryker as regulatory consultant.

Stryker Corporate is one of 440 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Stryker Corporate

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Sep 18, 2026