Zhejiang Chuangxiang Medical Technology Co., Ltd. FDA Approvals

0 new drug approvals and 9 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
Single Use Ureteral Access Sheath510(k)Sep 11, 2026Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Special)	Sep 11, 2026
Single use stone retrieval balloons510(k)Mar 6, 2026Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Mar 6, 2026
Disposable Ureteral Stents510(k)Feb 20, 2026Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Feb 20, 2026
Endoscopy Irrigation Tubing510(k)Nov 21, 2023Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Nov 21, 2023
Air/Water Bottle Tubing, CO2 Source Tubing510(k)Sep 8, 2023Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Sep 8, 2023
Single Use Cytology Brush510(k)Jul 28, 2022Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Jul 28, 2022
Single Use Hemoclip510(k)May 27, 2022Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	May 27, 2022
Single Use Ureteral Access Sheath510(k)May 25, 2022Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	May 25, 2022
Sclerotherapy Needle510(k)Feb 23, 2022Gastroenterology, Urology	Gastroenterology, Urology	510(k)Substantially Equivalent (Traditional)	Feb 23, 2022