Zhejiang Curaway Medical Technology Co., Ltd. FDA Approvals

0 new drug approvals and 7 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Automatic Core Biopsy Instrument510(k)Aug 28, 2026Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Aug 28, 2026
Disposable Biopsy Needle510(k)Jul 22, 2025Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Jul 22, 2025
Automatic Core Biopsy Instrument/ Semi-Automatic Core Biopsy Instrument/ Disposable Coaxial Biopsy Needle510(k)Jan 24, 2025Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Jan 24, 2025
Bone Marrow Biopsy Needle510(k)Jan 24, 2025Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Jan 24, 2025
Radiofrequency Generator System, Cura RF Electrode510(k)Dec 11, 2024General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Dec 11, 2024
Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter510(k)May 30, 2024General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	May 30, 2024
Irreversible Electroporation Ablation Generator, Irreversible Electroporation Probe510(k)Jun 8, 2023General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Jun 8, 2023