# Cogent Spine, LLC

- Location (FDA's records): Solana Beach, CA
- FDA decisions: 3 (2014–2016): 3 510(k) clearances
- Product codes: MAX (3)
- Predicates its devices cite: 7 (3 its own); citations of its devices by later devices: 4 (3 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
- Eisertech, LLC: 1 (https://510kreport.com/company/eisertech)
- Stryker Spine: 1 (https://510kreport.com/company/stryker-spine)
- Custom Spine, Inc.: 1 (https://510kreport.com/company/custom-spine)
- Sapphire Medical Group: 1 (https://510kreport.com/company/sapphire-medical-group)

## Firms that cite its devices most
- Genesys Spine: 1 (https://510kreport.com/company/genesys-spine)

## Its most-cited devices
- K132738: Cogent Med-Lif (2014), cited by 2
- K151406: Cogent Lateral Interbody System (2016), cited by 1
- K142193: Cogent Med-Lif XL (2014), cited by 1

## Recent decisions
- K151406: Cogent Lateral Interbody System (Feb 25, 2016)
- K142193: Cogent Med-Lif XL (Oct 15, 2014)
- K132738: Cogent Med-Lif (Apr 15, 2014)

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