FDA applicant
Medlog GmbH Marketing Services
FDA records 5 decisions for Medlog GmbH Marketing Services (Mchenry, IL) from 1981 to 1983: 5 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and BTT (Humidifier, Respiratory Gas, (Direct Patient…). 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 Medlog GmbH Marketing Services’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Medlog GmbH Marketing Services since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Medlog GmbH Marketing Services’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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