# Companion Spine France

- Location (FDA's records): Merignac
- FDA decisions: 4 (2009–2025): 1 510(k) clearance and 3 original PMA approvals
- Names in FDA's records: Companion Spine France (2); Companion Spine France Sas (2)
- Product codes: NQO (2), QLR (1), MJO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Empirical Spine, Inc.: 1 (https://510kreport.com/company/empirical-spine)

## Its most-cited devices
- K253118: Companion Spine DIAM™ Instrumentation (2025), cited by 1

## Recent decisions
- K253118: Companion Spine DIAM™ Instrumentation (Dec 16, 2025)
- P240043: DIAM­™ Spinal Stabilization System (Dec 10, 2025)
- P110008: Coflex® Interlaminar Technology (Oct 17, 2012)
- P060023: Bryan Cervical Disc Prosthesis (May 12, 2009)

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