FDA applicant

Dioptics

Irvine, CA6 decisions1986–19900 recalls

FDA records 6 decisions for Dioptics (Irvine, CA) from 1986 to 1990: 6 510(k) clearances. Most are in product codes HQY (Sunglasses (Non-Prescription Including…) and FXX (Mask, Surgical). 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 Dioptics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dioptics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Dioptics”

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

Dioptics Medical Products, Inc. 1

Dioptics

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dioptics”