Spine Innovation, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spine Innovation, LLC - FDA 510(k) Cleared Devices
Recent clearances: Titanium Interbody System
2
Total
2
Cleared
0
Denied
Spine Innovation, LLC has 2 FDA 510(k) cleared medical devices. Based in Solana Beach, US.
Latest FDA clearance: Jan 2026. Active since 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spine Innovation, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spine Innovation, LLC
2 devices