FDA applicant
Miami Eye Technology, Inc.
FDA records 6 decisions for Miami Eye Technology, Inc. (Mchenry, IL) from 1983 to 1984: 6 510(k) clearances. Most are in product codes HNY (Cystotome) and HJO (Biomicroscope, Slit-Lamp, Ac-Powered). 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 Miami Eye Technology, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Miami Eye Technology, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Miami Eye Technology, Inc.’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 “Miami”
FDA records each applicant name separately; these may or may not be the same firm.