510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K251890Substantially Equivalent

Disposable Ureteral Stents

Zhejiang Chuangxiang Medical Technology Co., Ltd., Hangzhou, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K251890 is the FDA 510(k) clearance record for Disposable Ureteral Stents, a class II device, cleared for Zhejiang Chuangxiang Medical Technology Co., Ltd. on under FDA product code FAD (Stent, Ureteral). FDA records list 13 510(k) clearances for Zhejiang Chuangxiang Medical Technology Co., Ltd., from to . As of , FDA records show no recalls naming K251890.

Clearance record

Decision date
Received
(245 days to decision)
Product code
FAD Stent, Ureteral
Regulation
21 CFR 876.4620
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Zhejiang Chuangxiang Medical Technology Co., Ltd. Rm. 101-1, 201-1, 301, 401, Bldg. 50, #650 Hongfeng Rd., Hangzhou, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FAD

Trailing 12 months
2 clearances under product code FAD in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FAD, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260