Wuxi Beien Surgery Device Co., Ltd.

Wuxi Beien Surgery Device Co., Ltd. holds 1 FDA 510(k) medical device clearance, cleared in 2022.

Top product codes for Wuxi Beien Surgery Device Co., Ltd.

GDW — General, Plastic Surgery1 device

Recent clearances by Wuxi Beien Surgery Device Co., Ltd.

K211811 — Disposable Endoscopic Staplers and Reload Unit, Disposable Hemorrhoidal Cutter Staplers, Disposable Linear Cutter Staplers, Disposable Circular StaplersCode GDW·2022-03-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.