# Integra Spine (Integra Lifesciences)

- Location (FDA's records): Medina, OH
- FDA decisions: 1 (2012–2012): 1 510(k) clearance
- Product codes: MAX (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 3 (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 whose devices it cites most
- Theken Spine, LLC: 1 (https://510kreport.com/company/theken-spine)

## Firms that cite its devices most
- SeaSpine Orthopedics Corporation: 1 (https://510kreport.com/company/seaspine-orthopedics)
- Seaspine, Inc.: 1 (https://510kreport.com/company/seaspine)
- Centinel Spine, Inc.: 1 (https://510kreport.com/company/centinel-spine)

## Its most-cited devices
- K112986: Lateral Fusion Device (2012), cited by 3

## Recent decisions
- K112986: Lateral Fusion Device (May 1, 2012)

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