Medical Device Manufacturer · US , Wayne , PA

Camber Spine Technologies, LLC - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2018

Total

Cleared

Denied

Camber Spine Technologies, LLC has 6 FDA 510(k) cleared medical devices. Based in Wayne, US.

Latest FDA clearance: Apr 2024. Active since 2018. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Camber Spine Technologies, LLC Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by MRC Global and MRC Global, LLC.

FDA 510(k) Regulatory Record - Camber Spine Technologies, LLC

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 10, 2026