Medical Device Manufacturer · US , Salt Lake City , UT

Nexus Spine - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
1
Total
1
Cleared
0
Denied

Nexus Spine has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.

Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Nexus Spine

1 devices
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