# Zefon Intl.

- Location (FDA's records): Ocala, FL
- FDA decisions: 2 (2008–2008): 2 510(k) clearances
- Product codes: DXQ (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K082630: Vitalcheck Blood Pressure Cuff, Model ZVC4000 Series (Dec 19, 2008)
- K080366: Duracheck Blood Pressure Cuff, Model ZDC4000 Series (Jun 9, 2008)

Source page: https://510kreport.com/company/zefon-intl