Nexus Spine, LLC - FDA 510(k) Cleared Devices

Nexus Spine, LLC has 17 FDA 510(k) cleared orthopedic devices. Based in Salt Lake City, US.

Latest FDA clearance: Apr 2025. Active since 2014.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

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