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FDA 510(k)

Disposable Ureteral Stents

K-Number: K251890 · 2026-02-20

ApplicantZhejiang Chuangxiang Medical Technology Co., Ltd.
Decision Date2026-02-20
Product CodeFAD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Disposable Ureteral Stents is a medical device manufactured by Zhejiang Chuangxiang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-02-20 under approval number K251890. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Disposable Ureteral Stents?

Disposable Ureteral Stents is a medical device that received FDA 510(k) clearance on 2026-02-20. It is manufactured by Zhejiang Chuangxiang Medical Technology Co., Ltd.. The 510(k) number is K251890.

When was Disposable Ureteral Stents approved by the FDA?

Disposable Ureteral Stents received FDA 510(k) clearance on 2026-02-20, under approval number K251890.

What company makes Disposable Ureteral Stents?

Disposable Ureteral Stents is manufactured by Zhejiang Chuangxiang Medical Technology Co., Ltd..

What is the FDA product code for Disposable Ureteral Stents?

The FDA product code for Disposable Ureteral Stents is FAD.

Related Clinical Trials

NCT07580963 Stent Related Symptoms Defined by Ureteral Stent Symptom Questionnaire in Patients With Image-Informed Ureteral Stent Lengths NOT_YET_RECRUITING NCT06045962 Optimal Stent Duration After Ureteroscopy ACTIVE_NOT_RECRUITING

Other Devices by Zhejiang Chuangxiang Medical Technology Co., Ltd.

K173758Disposable Biopsy Valve K172762Single Use Hemoclip K172758Rotatable Snares, Non-Rotatable Snares K192258Disposable Valve Sets K191900Single Use Grasping Forceps K220063Single Use Cytology Brush

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Related Devices (Code: FAD)

K163068pAguaMedicina PERSISTENT Structural Hydrogel Ureteral StentQ Urological Corporation K161277ConvertX Nephroureteral Stent SystemBrightwater Medical K160891Ultrathane Endoureterotomy Stent SetCook Incorporated K151051Universa Soft Ureteral Stents and Stent SetsCook Incorporated K170362VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENTSColoplast Corp. K170422BIOSOFT DUO DOUBLE LOOP URETERAL STENTSColoplast Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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