FDA applicant
Michael Onufryk
FDA records 1 decision for Michael Onufryk (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code HPA (Frame, Trial, 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 Michael Onufryk’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Michael Onufryk since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Michael Onufryk’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Michael”
FDA records each applicant name separately; these may or may not be the same firm.