# Codan US Corp.

- Location (FDA's records): Santa Ana, CA
- FDA decisions: 7 (1999–2012): 7 510(k) clearances
- Product codes: FPA (5), KNT (1), LHI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- B.Braun Medical, Inc.: 1 (https://510kreport.com/company/b-braun-medical)
- Vidacare Corporation: 1 (https://510kreport.com/company/vidacare)
- Nephros, Inc.: 1 (https://510kreport.com/company/nephros)

## Its most-cited devices
- K021480: Extension Set Light-Safe, Model BC565 (2002), cited by 2
- K033301: IV Administration and Connect Sets (2004), cited by 1

## Recent decisions
- K112268: Codan Safefeed Enteral Feeding Reservoir (Mar 19, 2012)
- K042693: IV Administration Set B400 SP (Oct 21, 2004)
- K033301: IV Administration and Connect Sets (Mar 4, 2004)
- K021480: Extension Set Light-Safe, Model BC565 (Jun 27, 2002)
- K013714: Codan US I.V. Administration Set, Model B400 SP (Mar 28, 2002)
- K001872: I.V. Set-Luer Lock with Latex Free Injection Site, Model B411 (Sep 7, 2000)
- K990711: Codan Chemospike (Apr 13, 1999)

Source page: https://510kreport.com/company/codan-us