FDA applicant
Optical Radiation Corp.
FDA records 3 decisions for Optical Radiation Corp. (Azusa, CA) from 1985 to 1992: 3 510(k) clearances. Most are in product codes HKX (Tonometer, Ac-Powered) and HLQ (Keratoscope, 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 Optical Radiation Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Optical Radiation Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Optical Radiation Corp.’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 “Optical”
FDA records each applicant name separately; these may or may not be the same firm.