510(k) Report

FDA applicant

Jiangsu Everyguard Plastic Products Co., Ltd.

Beijing, CN2 decisions2006–20060 recalls

FDA records 2 decisions for Jiangsu Everyguard Plastic Products Co., Ltd. (Beijing, CN) in 2006: 2 510(k) clearances. All are in product code LYZ (Vinyl Patient Examination Glove). 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, general hospital panel, where it files most

How often FDA has decided Jiangsu Everyguard Plastic Products Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jiangsu Everyguard Plastic Products Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Jiangsu Everyguard Plastic Products Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Jiangsu Everyguard Plastic Products…’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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