510(k) Report

FDA applicant

Top Glove (Zhangjiagang) Co., Ltd.

Xi Zhang Town, CN2 decisions2003–20030 recalls

FDA records 2 decisions for Top Glove (Zhangjiagang) Co., Ltd. (Xi Zhang Town, CN) in 2003: 2 510(k) clearances. All are in product code LYZ (Vinyl Patient Examination Glove). 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 Top Glove (Zhangjiagang) Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Top Glove (Zhangjiagang) Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Top Glove (Zhangjiagang) Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Top Glove (Zhangjiagang) 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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