# Johnson and Johnson

- Location (FDA's records): Raynham, MA
- FDA decisions: 2 (2011–2014): 2 510(k) clearances
- Product codes: MAX (1), KWP (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Depuy Spine, Inc.: 2 (https://510kreport.com/company/depuy-spine)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)

## Firms that cite its devices most
- Medos International SARL: 3 (https://510kreport.com/company/medos-international)
- Bright Spine: 1 (https://510kreport.com/company/bright-spine)

## Its most-cited devices
- K103488: Concorde Bullet Cage System (2011), cited by 4

## Recent decisions
- K142460: EXPEDIUM Spine System/Synapse System (Oct 1, 2014)
- K103488: Concorde Bullet Cage System (Mar 2, 2011)

Source page: https://510kreport.com/company/johnson-and-johnson