510(k) Report

FDA applicant

Shijiazhuang Brethern Plastic Co., Ltd.

Shijiazhuang, Hebei, CN2 decisions1999–19990 recalls

FDA records 2 decisions for Shijiazhuang Brethern Plastic Co., Ltd. (Shijiazhuang, Hebei, CN) in 1999: 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 Brethern Plastic Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Shijiazhuang Brethern Plastic Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Shijiazhuang Brethern Plastic Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Shijiazhuang”

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