FDA applicant
Dr. K. Honle GmbH
FDA records 3 decisions for Dr. K. Honle GmbH (Walker, MI) in 1983: 3 510(k) clearances. 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 Dr. K. Honle GmbH’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Dr. K. Honle GmbH since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Dr. K. Honle 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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