# Spine Innovation, LLC

- Location (FDA's records): Coronado, CA
- FDA decisions: 2 (2016–2026): 2 510(k) clearances
- Product codes: MAX (2)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Globus Medical, Inc.: 1 (https://510kreport.com/company/globus-medical)
- Eisertech, LLC: 1 (https://510kreport.com/company/eisertech)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)
- Alphatec Spine, Inc.: 1 (https://510kreport.com/company/alphatec-spine)
- Seaspine, Inc.: 1 (https://510kreport.com/company/seaspine)

## Its most-cited devices
- K153356: Spine Innovation Interbody System (2016), cited by 1

## Recent decisions
- K253266: Titanium Interbody System (Jan 8, 2026)
- K153356: Spine Innovation Interbody System (Jan 14, 2016)

Source page: https://510kreport.com/company/spine-innovation