# Zhejiang Curaway Medical Technology Co., Ltd.

- Location (FDA's records): Hangzhou, CN
- FDA decisions: 7 (2023–2026): 7 510(k) clearances
- Product codes: KNW (4), GEI (2), OAB (1)
- 510(k) review time since 2016: median 212 days, against 152 for FDA's reviews in the same codes and years (1 of 6 faster)
- Predicates its devices cite: 12 (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
- Bard Peripheral Vascular, Inc.: 2 (https://510kreport.com/company/bard-peripheral-vascular)
- Care Fusion: 2 (https://510kreport.com/company/care-fusion)
- Vnus Medical Technologies, Inc.: 2 (https://510kreport.com/company/vnus-medical-technologies)
- Starmed Co., Ltd.: 2 (https://510kreport.com/company/starmed)
- Gallini Intl., Inc.: 1 (https://510kreport.com/company/gallini-intl)
- Promisemed Hangzhou Meditech Co., Ltd.: 1 (https://510kreport.com/company/promisemed-hangzhou-meditech)
- AngioDynamics, Inc.: 1 (https://510kreport.com/company/angiodynamics)
- Merit Medical Systems, Inc.: 1 (https://510kreport.com/company/merit-medical-systems)

## Recent decisions
- K260517: Automatic Core Biopsy Instrument (Aug 28, 2026)
- K244018: Disposable Biopsy Needle (Jul 22, 2025)
- K241793: Automatic Core Biopsy Instrument/ Semi-Automatic Core Biopsy Instrument/ Disposable Coaxial Biopsy Needle (Jan 24, 2025)
- K242322: Bone Marrow Biopsy Needle (Jan 24, 2025)
- K240758: Radiofrequency Generator System, Cura RF Electrode (Dec 11, 2024)
- K232505: Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter (May 30, 2024)
- K222001: Irreversible Electroporation Ablation Generator, Irreversible Electroporation Probe (Jun 8, 2023)

Source page: https://510kreport.com/company/zhejiang-curaway-medical-technology