FDA applicant
Rud Riester GmbH & CO KG
FDA records 4 decisions for Rud Riester GmbH & CO KG (Jungingen, DE) in 1994: 4 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and LDE (Stethoscope, Manual). 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 Rud Riester GmbH & CO KG’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Rud Riester GmbH & CO KG since 2007.
Recalls per year
No recall linked to its devices since 2007.
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