FDA applicant
Artos Medical Products GmbH
FDA records 4 decisions for Artos Medical Products GmbH (Indianapolis, IN) in 1996: 4 510(k) clearances. Most are in product codes JDI (Prosthesis, Hip, Semi-Constrained…) and LWJ (Prosthesis, Hip, Semi-Constrained…). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Artos Medical Products GmbH’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Artos Medical Products GmbH since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Artos Medical Products GmbH’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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