FDA applicant

Metro Optics, Inc.

Grand Junction, CO1 decision2003–20030 recalls

FDA records 1 decision for Metro Optics, Inc. (Grand Junction, CO) in 2003: 1 510(k) clearance. All are in product code HQD (Lens, Contact (Other Material) - Daily). Its devices cite 1 predicate, 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 Metro Optics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Metro Optics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Metro”

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

Metro Optics of Austin, Inc. 8 Metro. Hospital & Health Center 1 Metro Medical Equipment, Inc. 1 Metro-Care 1

Metro Optics, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Metro”