Company ยท CN
Zhejiang Curaway Medical Technology Co., Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2023 to 2026. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 28, 2026 | K260517 | Automatic Core Biopsy Instrument Zhejiang Curaway Medical Technology Co., Ltd., CN | KNW |
| Jul 22, 2025 | K244018 | Disposable Biopsy Needle Zhejiang Curaway Medical Technology Co., Ltd., CN | KNW |
| Jan 24, 2025 | K242322 | Bone Marrow Biopsy Needle Zhejiang Curaway Medical Technology Co., Ltd., CN | KNW |
| Jan 24, 2025 | K241793 | Automatic Core Biopsy Instrument/ Semi-Automatic Core Biopsy Instrument/ Disposable Coaxial Biopsy Needle Zhejiang Curaway Medical Technology Co., Ltd., CN | KNW |
| Dec 11, 2024 | K240758 | Radiofrequency Generator System, Cura RF Electrode Zhejiang Curaway Medical Technology Co., Ltd., CN | GEI |
| May 30, 2024 | K232505 | Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter Zhejiang Curaway Medical Technology Co., Ltd., CN | GEI |
| Jun 8, 2023 | K222001 | Irreversible Electroporation Ablation Generator, Irreversible Electroporation Probe Zhejiang Curaway Medical Technology Co., Ltd., CN | OAB |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||