FDA applicant
Friandent GmbH
FDA records 2 decisions for Friandent GmbH (Lake Forest, CA) in 2003: 2 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 2 predicates, 1 of them its own earlier devices. 3 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Friandent GmbH’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Friandent GmbH since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Friandent GmbH’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report