# Tfx Medical Group

- Location (FDA's records): Jeffrey, NH
- FDA decisions: 3 (1996–2000): 3 510(k) clearances
- Product codes: DQX (1), DRB (1), DYB (1)
- Predicates its devices cite: 20 (0 its own); citations of its devices by later devices: 5 (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
- Lake Region Mfg., Inc.: 8 (https://510kreport.com/company/lake-region-mfg)
- Teleflexmedical, Inc.: 3 (https://510kreport.com/company/teleflexmedical)
- Cook, Inc.: 3 (https://510kreport.com/company/cook)
- Arrow Intl., Inc.: 2 (https://510kreport.com/company/arrow-intl)
- Argon Medical Corp.: 2 (https://510kreport.com/company/argon-medical)
- Guidewire Technologies, Inc.: 2 (https://510kreport.com/company/guidewire-technologies)

## Firms that cite its devices most
- Mentor Medical Limited: 1 (https://510kreport.com/company/mentor-medical)
- Cardiosolutions, Inc.: 1 (https://510kreport.com/company/cardiosolutions)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)
- Emmebi Srl: 1 (https://510kreport.com/company/emmebi)
- Galt Medical Corp.: 1 (https://510kreport.com/company/galt-medical)

## Its most-cited devices
- K963320: TFX Medical Guidewire (1996), cited by 4
- K992664: TFX Medical Stylet Catheter (2000), cited by 1

## Recent decisions
- K992664: TFX Medical Stylet Catheter (Apr 13, 2000)
- K991647: TFX Medical Introducer Kit (Jan 4, 2000)
- K963320: TFX Medical Guidewire (Dec 3, 1996)

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