510(k) Report

FDA applicant

Ningbo Yujiang Plastic & Rubber Co., Ltd.

Green Valley, AZ4 decisions1989–20010 recalls

FDA records 4 decisions for Ningbo Yujiang Plastic & Rubber Co., Ltd. (Green Valley, AZ) from 1989 to 2001: 4 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and LZA (Polymer 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 Ningbo Yujiang Plastic & Rubber Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ningbo Yujiang Plastic & Rubber Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ningbo Yujiang Plastic & Rubber Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Ningbo Yujiang Plastic & Rubber Co.…’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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