FDA applicant
F. & F. Koenigkramer
FDA records 9 decisions for F. & F. Koenigkramer (Mchenry, IL) from 1977 to 1986: 9 510(k) clearances. Most are in product codes HME (Chair, Ophthalmic, Ac-Powered) and HQF (Laser, Ophthalmic). 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 F. & F. Koenigkramer’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for F. & F. Koenigkramer since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like F. & F. Koenigkramer’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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