# Cefla S.C.R.L.

- Location (FDA's records): Ormond Beach, FL
- FDA decisions: 3 (2006–2008): 3 510(k) clearances
- Product codes: MUH (1), EIA (1), EHD (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 3 (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
- Visiodent SA: 1 (https://510kreport.com/company/visiodent)
- Air Techniques, Inc.: 1 (https://510kreport.com/company/air-techniques)
- Julie Alliance: 1 (https://510kreport.com/company/julie-alliance)

## Firms that cite its devices most
- Cefla Dental Group: 1 (https://510kreport.com/company/cefla-dental-group)
- Dentron Systems, LLC: 1 (https://510kreport.com/company/dentron-systems)
- Cefla S.C.: 1 (https://510kreport.com/company/cefla-sc)

## Its most-cited devices
- K061114: WDS, Size 2 and Size 2 (2006), cited by 2
- K080076: RX DC X-Ray Unit (2008), cited by 1

## Recent decisions
- K080076: RX DC X-Ray Unit (Mar 14, 2008)
- K062897: C-U2 (Dec 14, 2006)
- K061114: WDS, Size 2 and Size 2 (Jun 6, 2006)

Source page: https://510kreport.com/company/cefla-scrl