# Leventon, S.A.

- Location (FDA's records): Barcelona, ES
- FDA decisions: 5 (1985–2005): 5 510(k) clearances
- Product codes: BWF (2), FPA (1), LDR (1), MEB (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (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 whose devices it cites most
- Dhd Diemolding Healthcare Div.: 1 (https://510kreport.com/company/dhd-diemolding-healthcare-div)

## Firms that cite its devices most
- Victus, Inc.: 1 (https://510kreport.com/company/victus)

## Its most-cited devices
- K952810: Dosi-Flow, Models 20 & 30 (1995), cited by 1

## Recent decisions
- K053149: Spiro-Ball (Dec 13, 2005)
- K040752: Dosi-Fuser (Apr 7, 2004)
- K994074: Tri-Ball (Jun 8, 2000)
- K952810: Dosi-Flow, Models 20 & 30 (Sep 8, 1995)
- K851058: Dosi Flow (Apr 29, 1985)

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