# Beijing Zksk Technology Co., Ltd.

- Location (FDA's records): Beijing, CN
- FDA decisions: 6 (2022–2025): 6 510(k) clearances
- Product codes: KGE (1), PKL (1), FDI (1), KNS (1), FBK (1), FHN (1)
- 510(k) review time since 2016: median 248 days, against 230 for FDA's reviews in the same codes and years (0 of 4 faster)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Anrei Medical (Hangzhou) Co., Ltd.: 2 (https://510kreport.com/company/anrei-medical-hangzhou)
- Olympus Medical Systems Corp.: 1 (https://510kreport.com/company/olympus-medical-systems)
- Zhejiang Chuangxiang Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/zhejiang-chuangxiang-medical-technology)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Wilson-Cook Medical, Inc.: 1 (https://510kreport.com/company/wilson-cook-medical)

## Recent decisions
- K242192: Disposable Sphincterotome (Feb 6, 2025)
- K231721: Disposable Hot Biopsy Forceps (Dec 14, 2023)
- K213217: Disposable hemoclip (Nov 14, 2022)
- K213222: Disposable Polypectomy Snare (Jun 6, 2022)
- K213223: Multi-Band Ligator (Jun 6, 2022)
- K213239: Endoscopic Injection Needle (Jun 2, 2022)

Source page: https://510kreport.com/company/beijing-zksk-technology