510(k) Report

FDA applicant

Shandong Jiazhan Plastic Products Co., Ltd.

Sparks, NV2 decisions2002–20020 recalls

FDA records 2 decisions for Shandong Jiazhan Plastic Products Co., Ltd. (Sparks, NV) in 2002: 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 Shandong Jiazhan Plastic Products Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Shandong Jiazhan Plastic Products Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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