FDA applicant

Medartis Medizinprodukte Und Forschung AG

Alling, DE1 decision2005–20050 recalls

FDA records 1 decision for Medartis Medizinprodukte Und Forschung AG (Alling, DE) in 2005: 1 510(k) clearance. All are in product code MQV (Filler, Bone Void, Calcium Compound). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Medartis Medizinprodukte Und Forschung AG’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medartis Medizinprodukte Und Forschung AG since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medartis Medizinprodukte Und Forschung AG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Medartis”

FDA records each applicant name separately; these may or may not be the same firm.

Medartis AG 47

Medartis Medizinprodukte Und Forschung AG

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medartis”