510(k) Report

FDA applicant

Wenzhou Wuzhou Import & Export Co., Ltd.

Bingyi Xiang, Zhejiang, CN2 decisions2011–20140 recalls

FDA records 2 decisions for Wenzhou Wuzhou Import & Export Co., Ltd. (Bingyi Xiang, Zhejiang, CN) from 2011 to 2014: 2 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and FMI (Needle, Hypodermic, Single Lumen). 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 Wenzhou Wuzhou Import & Export Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2011: 12014: 1
2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Wenzhou Wuzhou Import & Export Co., Ltd. by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Wenzhou Wuzhou Import & Export 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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