510(k) Report

FDA applicant

Wuxi Yushou Medical Applicances Co., Ltd.

Wuxi, CN3 decisions2006–20130 recalls

FDA records 3 decisions for Wuxi Yushou Medical Applicances Co., Ltd. (Wuxi, CN) from 2006 to 2013: 3 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and FMI (Needle, Hypodermic, Single Lumen). Its devices cite 5 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 Wuxi Yushou Medical Applicances Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2013

2013: 2
2007high 2 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Wuxi Yushou Medical Applicances Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Wuxi”

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