FDA applicant
Stierlen-Maquet AG
FDA records 10 decisions for Stierlen-Maquet AG (West Germany, GR) from 1984 to 1997: 10 510(k) clearances. Most are in product codes JEB (Table, Surgical With Orthopedic Accessories…) and GDC (Table, Operating-Room, Electrical). 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 Stierlen-Maquet AG’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Stierlen-Maquet AG since 2007.
Recalls per year
No recall linked to its devices since 2007.
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