# Teleflex Medical Group

- Location (FDA's records): Jaffrey, NH
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: JDW (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 4 (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, Inc.: 1 (https://510kreport.com/company/depuy)
- New Deal, S.A.: 1 (https://510kreport.com/company/new-deal)

## Firms that cite its devices most
- Trilliant Surgical, Ltd.: 2 (https://510kreport.com/company/trilliant-surgical)
- Verticor, Ltd.: 1 (https://510kreport.com/company/verticor)
- Evergreen Orthopedic Research Lab: 1 (https://510kreport.com/company/evergreen-orthopedic-research-lab)

## Its most-cited devices
- K030336: Kmedic External Fixation Devices (2003), cited by 4

## Recent decisions
- K030336: Kmedic External Fixation Devices (Mar 6, 2003)

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