# Friandent GmbH

- Location (FDA's records): Lake Forest, CA
- FDA decisions: 2 (2003–2003): 2 510(k) clearances
- Product codes: DZE (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Friadent GmbH: 1 (https://510kreport.com/company/friadent)

## Firms that cite its devices most
- Intra-Lock International: 1 (https://510kreport.com/company/intra-lock-international)

## Its most-cited devices
- K030639: Xive 3.0 Dental Implant System (2003), cited by 2

## Recent decisions
- K032750: Modification to: Xive 3.0 Dental Implant System, Multiple (Oct 2, 2003)
- K030639: Xive 3.0 Dental Implant System (Aug 12, 2003)

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