# Surfix Technologies

- Location (FDA's records): Potomac, MD
- FDA decisions: 1 (2004–2004): 1 510(k) clearance
- Product codes: HRS (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (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
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)

## Firms that cite its devices most
- Newclip Technics: 2 (https://510kreport.com/company/newclip-technics)
- Neosteo: 1 (https://510kreport.com/company/neosteo)

## Its most-cited devices
- K041601: Surfix Knee Osteotomy System (2004), cited by 3

## Recent decisions
- K041601: Surfix Knee Osteotomy System (Aug 27, 2004)

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