# Fixano SA

- Location (FDA's records): La Jolla, CA
- FDA decisions: 5 (2001–2002): 5 510(k) clearances
- Product codes: KTT (4), HTY (1)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 1 (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
- Ferguson Medical: 1 (https://510kreport.com/company/ferguson-medical)
- Ebi, L.P.: 1 (https://510kreport.com/company/ebi)
- Depuy, Inc.: 1 (https://510kreport.com/company/depuy)
- Syntec Scientific Corp.: 1 (https://510kreport.com/company/syntec-scientific)
- Danek Medical, Inc.: 1 (https://510kreport.com/company/danek-medical)
- Orthopaedic Innovations, Inc.: 1 (https://510kreport.com/company/orthopaedic-innovations)

## Its most-cited devices
- K012062: PF2 (2001), cited by 1

## Recent decisions
- K023314: Microfix (Oct 18, 2002)
- K022771: Twin Fix (Sep 23, 2002)
- K012062: PF2 (Sep 27, 2001)
- K012078: Radiofix (Sep 27, 2001)
- K012161: Flex-Nails (Aug 24, 2001)

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