# Cefar Medical AB

- Location (FDA's records): Minneapolis,, MN
- FDA decisions: 2 (2002–2003): 2 510(k) clearances
- Product codes: GZJ (1), IPF (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (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
- Rehabilicare, Inc.: 2 (https://510kreport.com/company/rehabilicare)

## Firms that cite its devices most
- Newlife Sciences, LLC: 1 (https://510kreport.com/company/newlife-sciences)
- Mediphysics Pain Centers of America: 1 (https://510kreport.com/company/mediphysics-pain-centers-of-america)

## Its most-cited devices
- K020803: Cefar Medical AB Cefar Primo (2002), cited by 2

## Recent decisions
- K030403: Cefar Rehab 2 and Rehab 2 Pro (Jul 17, 2003)
- K020803: Cefar Medical AB Cefar Primo (Jun 10, 2002)

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