FDA applicant

Ocu-Ease Optical Products, Inc.

Pinole, CA9 decisions1994–20020 recalls

FDA records 9 decisions for Ocu-Ease Optical Products, Inc. (Pinole, CA) from 1994 to 2002: 9 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 7 predicates, 0 of them its own earlier devices. 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 Ocu-Ease Optical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ocu-Ease Optical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ocu-Ease Optical Products, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?