# Mentor Medical Limited

- Location (FDA's records): Hyth, Kent, GB
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: JOH (1)
- Predicates its devices cite: 7 (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
- Smiths Industries Medical Systems, Inc.: 3 (https://510kreport.com/company/smiths-industries-medical-systems)
- Rusch Intl.: 1 (https://510kreport.com/company/rusch-intl)
- Mallinckroot, Inc.: 1 (https://510kreport.com/company/mallinckroot)
- Pharma-Plast USA, Inc.: 1 (https://510kreport.com/company/pharma-plast-usa)
- Tfx Medical Group: 1 (https://510kreport.com/company/tfx-medical-group)

## Firms that cite its devices most
- Cook, Inc.: 1 (https://510kreport.com/company/cook)
- Portex, Inc.: 1 (https://510kreport.com/company/portex)
- Smiths Medical: 1 (https://510kreport.com/company/smiths-medical)

## Its most-cited devices
- K022212: Portex Percutaneous Dilatational Tracheostomy Kits (2003), cited by 3

## Recent decisions
- K022212: Portex Percutaneous Dilatational Tracheostomy Kits (Mar 21, 2003)

Source page: https://510kreport.com/company/mentor-medical