Medical Device Manufacturer · US , Carlsbad , CA

SeaSpine Orthopedics Corporation - FDA 510(k) Cleared Devices

67 submissions · 67 cleared · Since 2016

Recent clearances: Admiral ACP System, Virata Spinal Fixation System, FLASH™ Facet Fusion Instruments, IsoTis® Facet Fusion Instruments

67
Total
67
Cleared
0
Denied

SeaSpine Orthopedics Corporation has 67 FDA 510(k) cleared orthopedic devices. Based in Carlsbad, US.

Latest FDA clearance: Jul 2026. Active since 2016.

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 7D Surgical ULC as regulatory consultant.

FDA 510(k) Regulatory Record - SeaSpine Orthopedics Corporation

67 devices
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