FDA applicant
Ascon Medical Instruments, Ltd.
FDA records 6 decisions for Ascon Medical Instruments, Ltd. (Westmont, IL) in 1985: 6 510(k) clearances. Most are in product codes HPA (Frame, Trial, Ophthalmic) and HNR (Forceps, 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 Ascon Medical Instruments, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Ascon Medical Instruments, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Ascon Medical Instruments, Ltd.’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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