510(k) Report

FDA applicant

Wei Fang Jiuzhou Gloves Co., Ltd.

Beijing, Haidian Distric, CN2 decisions2006–20060 recalls

FDA records 2 decisions for Wei Fang Jiuzhou Gloves Co., Ltd. (Beijing, Haidian Distric, CN) in 2006: 2 510(k) clearances. All are in product code LYZ (Vinyl Patient Examination Glove). Its devices cite 2 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, general hospital panel, where it files most

How often FDA has decided Wei Fang Jiuzhou Gloves Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wei Fang Jiuzhou Gloves Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Wei Fang Jiuzhou Gloves Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Wei Fang Jiuzhou Gloves 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?

  • LYZVinyl Patient Examination Glove2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K060884Powder-Free Vinyl Patient Examination GlovesWei Fang Jiuzhou Gloves Co., Ltd. · 2006
  • K060886Powdered Vinyl Patient Examination GlovesWei Fang Jiuzhou Gloves Co., Ltd. · 2006

All 2 as Wei Fang Jiuzhou Gloves Co., Ltd. →