# Depuy Mitek Inc., Johnson and Johnson Company

- Location (FDA's records): Raynham, MA
- FDA decisions: 1 (2012–2012): 1 510(k) clearance
- Product codes: MAI (1)
- Predicates its devices cite: 2 (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 whose devices it cites most
- Depuy Mitek, A Johnson & Johnson Company: 2 (https://510kreport.com/company/depuy-mitek-a-johnson-johnson)

## Firms that cite its devices most
- Depuy Mitek, A Johnson & Johnson Company: 1 (https://510kreport.com/company/depuy-mitek-a-johnson-johnson)

## Its most-cited devices
- K120078: Healix Advance BR Anchor (2012), cited by 1

## Recent decisions
- K120078: Healix Advance BR Anchor (Feb 29, 2012)

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