FDA applicant

Action Eyewear Corp.

Fort Collin, CO2 decisions1993–19930 recalls

FDA records 2 decisions for Action Eyewear Corp. (Fort Collin, CO) in 1993: 2 510(k) clearances. Most are in product codes LYU (Accessory, Surgical Apparel) and HOY (Shield, Eye, Ophthalmic (Including Sunlamp…). 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, general and plastic surgery panel, where it files most

How often FDA has decided Action Eyewear Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Action Eyewear Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Action”

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

Action Manufacturing, Inc. 3 Action Products, Inc. 2 Action Medical Systems, Inc. 2 Action Engineering, Inc. 1 Action Hygiene Products, Inc. 1 Action Labs, Inc. 1

Action Eyewear Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Action”