510(k) Report

FDA applicant

Shijiazhuang Tillotson Rubber Products Co., Ltd.

Brea, CA2 decisions2004–20050 recalls

FDA records 2 decisions for Shijiazhuang Tillotson Rubber Products Co., Ltd. (Brea, CA) from 2004 to 2005: 2 510(k) clearances. Most are in product codes LZA (Polymer Patient Examination Glove) and LYY (Latex Patient Examination Glove). Its devices cite 2 predicates, 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, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Shijiazhuang Tillotson Rubber Products Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Shijiazhuang Tillotson Rubber Products Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Shijiazhuang Tillotson Rubber Products…’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.