510(k) Report

FDA applicant

Optical Center

Oxnard, CA1 decision1988–19880 recalls

FDA records 1 decision for Optical Center (Oxnard, CA) in 1988: 1 510(k) clearance. All are in product code HNN (Knife, Ophthalmic). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ophthalmic panel, where it files most

How often FDA has decided Optical Center’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Optical Center since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Optical Center by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Optical”

FDA records each applicant name separately; these may or may not be the same firm.