FDA applicant
Ocular Instruments, Inc.
FDA records 50 decisions for Ocular Instruments, Inc. (Bellevue, WA) from 1984 to 2002: 50 510(k) clearances. Most are in product codes HJK (Lens, Contact, Polymethylmethacrylate…) and HKS (Prism, Gonioscopic). 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 Ocular Instruments, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Ocular Instruments, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Ocular Instruments, 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 “Ocular”
FDA records each applicant name separately; these may or may not be the same firm.