FDA applicant
Wenzhou Wuzhou Import & Export Co., Ltd.
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
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
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2011.
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.
See the 510(k) Report