510(k) Report

FDA applicant

Jinhua Latex Products Factory

Green Valley, AZ1 decision1997–19970 recalls

FDA records 1 decision for Jinhua Latex Products Factory (Green Valley, AZ) in 1997: 1 510(k) clearance. All are in product code LYY (Latex 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 Jinhua Latex Products Factory’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jinhua Latex Products Factory since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Jinhua Latex Products Factory by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Jinhua”

FDA records each applicant name separately; these may or may not be the same firm.