Nexus Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nexus Spine - FDA 510(k) Cleared Devices
Recent clearances: PressON Spinal Fixation System
2
Total
2
Cleared
0
Denied
Nexus Spine has 2 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Latest FDA clearance: Jun 2026. 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.
510(k) submissions have been managed by MRC Global as regulatory consultant.
FDA 510(k) Regulatory Record - Nexus Spine
2 devices