# Kfx Medical

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 7 (2006–2012): 7 510(k) clearances
- Product codes: MBI (7)
- Predicates its devices cite: 9 (3 its own); citations of its devices by later devices: 4 (3 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
- Arthrex, Inc.: 3 (https://510kreport.com/company/arthrex)
- Opus Medical, Inc.: 2 (https://510kreport.com/company/opus-medical)
- Linvatec Corp.: 1 (https://510kreport.com/company/linvatec)

## 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
- K072063: KFX Tissue Fixation System and Accessories (2007), cited by 2
- K081598: Suture Lock Nail Bone Anchor with White (KFX-W-200) & Blue (KFX-B-200) Fiberforce Suture (2008), cited by 1
- K061294: KFX Knotless Fixation System (2006), cited by 1

## Recent decisions
- K120841: Appianfx Suture Anchor (6MM) (5MM) Appianfx Tissue Anchor (Jun 7, 2012)
- K101175: KFX Appianfx Peek Femoral Implant with Inserter (May 20, 2010)
- K083609: KFX Peek Bone Anchor with Pre-Attached Sutures and Inserter Handle (Mar 6, 2009)
- K081598: Suture Lock Nail Bone Anchor with White (KFX-W-200) & Blue (KFX-B-200) Fiberforce Suture (Jul 3, 2008)
- K080229: 5.5 MM Suture Lock Bone Screw Anchor (Feb 29, 2008)
- K072063: KFX Tissue Fixation System and Accessories (Oct 26, 2007)
- K061294: KFX Knotless Fixation System (Jul 19, 2006)

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