510(k) Report

FDA applicant

Yeou-Fwu Rubber Industrial Co., Ltd.

Shiang,Chang Huahsie, TW2 decisions1989–19890 recalls

FDA records 2 decisions for Yeou-Fwu Rubber Industrial Co., Ltd. (Shiang,Chang Huahsie, TW) in 1989: 2 510(k) clearances. 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 Yeou-Fwu Rubber Industrial Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Yeou-Fwu Rubber Industrial Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Yeou-Fwu Rubber Industrial Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Yeou-Fwu Rubber Industrial Co., Ltd.’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 “Yeou-Fwu”

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