FDA applicant
Ningbo Yujiang Plastic & Rubber Co., Ltd.
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
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.
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