510(k) Report

FDA applicant

Shijiazhuang Huijingyuan Plastic Co, Ltd.

Greenwood Village, CO2 decisions2010–20100 recalls

FDA records 2 decisions for Shijiazhuang Huijingyuan Plastic Co, Ltd. (Greenwood Village, CO) in 2010: 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 Shijiazhuang Huijingyuan Plastic Co, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2010

2010: 2
2010high 2 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Shijiazhuang Huijingyuan Plastic Co, Ltd. by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Shijiazhuang”

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