510(k) Report

FDA applicant

Ya Mei Technology Co., Ltd.

Littleton, CO1 decision2003–20030 recalls

FDA records 1 decision for Ya Mei Technology Co., Ltd. (Littleton, CO) in 2003: 1 510(k) clearance. All are in product code KGO (Surgeon'S Gloves). 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 Ya Mei Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ya Mei Technology Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ya Mei Technology Co., Ltd.’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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Which product codes does it file in?

  • KGOSurgeon'S Gloves1decision

What has FDA decided for it lately?

  • K031130YA Mei First Aid KitYa Mei Technology Co., Ltd. · 2003

The one decision as Ya Mei Technology Co., Ltd. →