# Velopex International, Inc.

- Location (FDA's records): St. Cloud, FL
- FDA decisions: 3 (2003–2011): 3 510(k) clearances
- Product codes: IXW (2), KOJ (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 2 (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
- Dent-X Co.: 2 (https://510kreport.com/company/dent-x)

## Firms that cite its devices most
- Kavo America: 1 (https://510kreport.com/company/kavo-america)

## Its most-cited devices
- K093503: Intrax Film Processor (2010), cited by 1
- K024105: Velopex Aquacut Fluid Abrasion Unit (2003), cited by 1

## Recent decisions
- K111167: Xtender Film Processor, Sprint Film Processor Model Xtender Model Sprint (Aug 18, 2011)
- K093503: Intrax Film Processor (Jan 6, 2010)
- K024105: Velopex Aquacut Fluid Abrasion Unit (Oct 9, 2003)

Source page: https://510kreport.com/company/velopex-international