Medical Device Manufacturer · US , Washington , DC

Ortho Kinematics, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2011

Total

Cleared

Denied

Ortho Kinematics, Inc. has 6 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 6 cleared submissions from 2011 to 2017. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Ortho Kinematics, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

Ortho Kinematics, Inc. is one of 13679 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ortho Kinematics, Inc.

6 devices

1-6 of 6

Data Source

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

Last updated: Sep 14, 2026