ClearanceBrief
Company ยท CN

Beijing Zksk Technology Co., Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2022 to 2025. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FBKEndoscopic Injection Needle, Gastroenterology-Urology1
FDISnare, Flexible1
FHNLigator, Hemorrhoidal1
KGEForceps, Biopsy, Electric1
KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)1
PKLHemostatic Metal Clip For The Gi Tract1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 6, 2025K242192Disposable Sphincterotome
Beijing Zksk Technology Co., Ltd., CN
KNS
Dec 14, 2023K231721Disposable Hot Biopsy Forceps
Beijing Zksk Technology Co., Ltd., CN
KGE
Nov 14, 2022K213217Disposable hemoclip
Beijing Zksk Technology Co., Ltd., CN
PKL
Jun 6, 2022K213223Multi-Band Ligator
Beijing Zksk Technology Co., Ltd., CN
FHN
Jun 6, 2022K213222Disposable Polypectomy Snare
Beijing Zksk Technology Co., Ltd., CN
FDI
Jun 2, 2022K213239Endoscopic Injection Needle
Beijing Zksk Technology Co., Ltd., CN
FBK

Latest recalls

DateFirm and productCodeLinked 510(k)
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