# Afx, Inc.

- Location (FDA's records): Fremont, CA
- FDA decisions: 2 (2001–2002): 2 510(k) clearances
- Product codes: NEY (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 21 (1 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
- Cryogen, Inc.: 1 (https://510kreport.com/company/cryogen)
- Heartport, Inc.: 1 (https://510kreport.com/company/heartport)

## Firms that cite its devices most
- Epicor Medical, Inc.: 4 (https://510kreport.com/company/epicor-medical)
- Medtronic Vascular: 2 (https://510kreport.com/company/medtronic-vascular)
- Microsurgeon, Inc.: 2 (https://510kreport.com/company/microsurgeon)
- AtriCure, Inc.: 2 (https://510kreport.com/company/atricure)
- Medical, Inc.: 2 (https://510kreport.com/company/medical)
- Guidant Corporation, Cardiac Surgery: 2 (https://510kreport.com/company/guidant-cardiac-surgery)
- Foundry Newco X, Inc.: 1 (https://510kreport.com/company/foundry-newco-x)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)

## Its most-cited devices
- K003978: Afx Microwave Generator, Flex Ablation Wand, Lynx Ablation Wand, Model Series 1000, P/N 102006, P/N 102007 (2001), cited by 12
- K013946: Flex 10 Accessory for the Afx Microwave Ablation System (2002), cited by 9

## Recent decisions
- K013946: Flex 10 Accessory for the Afx Microwave Ablation System (Feb 27, 2002)
- K003978: Afx Microwave Generator, Flex Ablation Wand, Lynx Ablation Wand, Model Series 1000, P/N 102006, P/N 102007 (May 22, 2001)

Source page: https://510kreport.com/company/afx