510(k) Report

FDA applicant

Shijiazhuang Hongxiang Plastics Products Co., Ltd.

Chino, CA9 decisions1999–20061 recall

FDA records 9 decisions for Shijiazhuang Hongxiang Plastics Products Co., Ltd. (Chino, CA) from 1999 to 2006: 9 510(k) clearances. All are in product code LYZ (Vinyl Patient Examination Glove). Its devices cite 7 predicates, 1 of them its own earlier devices. 1 recall is linked to its devices.

FDA’s records also spell it “Shijiazhuang Hongxiang Plastics Products Co; , Ltd.”.

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 Shijiazhuang Hongxiang Plastics Products Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Shijiazhuang Hongxiang Plastics Products Co., Ltd. since 2007.

Recalls per year

1in 2009

2009: 1
2007high 1 (2009) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Shijiazhuang Hongxiang Plastics…’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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Other applicant names beginning “Shijiazhuang”

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