510(k) Report

FDA applicant

Walmart Stores

Bentonville, AR5 decisions1994–19950 recalls

FDA records 5 decisions for Walmart Stores (Bentonville, AR) from 1994 to 1995: 5 510(k) clearances. All are in product code HQY (Sunglasses (Non-Prescription Including…). 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 Walmart Stores’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Walmart Stores since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Walmart Stores’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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