# Difusion Technologies

- Location (FDA's records): Austin, TX
- FDA decisions: 3 (2010–2019): 3 510(k) clearances
- Product codes: MAX (3)
- Predicates its devices cite: 9 (2 its own); citations of its devices by later devices: 7 (2 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
- Sofamor Danek: 1 (https://510kreport.com/company/sofamor-danek)
- Zimmer Spine, Inc.: 1 (https://510kreport.com/company/zimmer-spine)
- Stryker Spine: 1 (https://510kreport.com/company/stryker-spine)
- Depuy Spine, Inc.: 1 (https://510kreport.com/company/depuy-spine)
- Ldr Spine USA: 1 (https://510kreport.com/company/ldr-spine-usa)
- Eminent Spine: 1 (https://510kreport.com/company/eminent-spine)
- Theken Spine, LLC: 1 (https://510kreport.com/company/theken-spine)

## Firms that cite its devices most
- K2m, Inc.: 1 (https://510kreport.com/company/k2m)
- Spineworks, LLC: 1 (https://510kreport.com/company/spineworks)
- Integrity Spine Lumbar Interbody Fusion System: 1 (https://510kreport.com/company/integrity-spine-lumbar-interbody-fusion-system)
- Thompson Mis, Inc.: 1 (https://510kreport.com/company/thompson-mis)
- Next Orthosurgical: 1 (https://510kreport.com/company/next-orthosurgical)

## Its most-cited devices
- K100042: Difusion Technologies Xiphos Interbody Fusion System (2010), cited by 6
- K123969: Xiphos (2013), cited by 1

## Recent decisions
- K190544: XIHPOS™ ZFUZE™ Interbody Fusion System (Nov 1, 2019)
- K123969: Xiphos (Feb 7, 2013)
- K100042: Difusion Technologies Xiphos Interbody Fusion System (Oct 1, 2010)

Source page: https://510kreport.com/company/difusion-technologies