510(k) Report

510(k) · Cleared

Cleared

Disposable Ureteral Stents

K251890510(k) TraditionalCleared Feb 20, 2026245-day reviewClass II21 CFR 876.4620

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Zhejiang Chuangxiang Medical Technology Co., Ltd. · FAD Stent, Ureteral

Cleared on Feb 20, 2026 as substantially equivalent to K161236 (Cook Incorporated, 2017) after a 245-day review. Its family tree reaches back 6 generations to 1991.

Decided
Feb 20, 2026
Review
245 days
Class
Class II
Product code
FAD
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K903345 (1991). 8 ancestors in all, the oldest K905289 (1991). No later device cites it as a predicate yet.

  1. Root · 6 generations backK903345 Bard (R) Lubricious - Coated Ureteral Stent SutureC.R. Bard, Inc. · 1991
  2. 5 generations backK983498 Bard Inlay Lubricious Double Pigtail Ureteral Stent with Suture…C.R. Bard, Inc. · 1998 · Recalled
  3. 4 generations backK022447 Bard ER Ureteral Stent with SutureC.R. Bard, Inc. · 2003
  4. 3 generations backK043193 Bard Inlayoptima Ureteral Stent with SutureC.R. Bard, Inc. · 2004 · Recalled
  5. 2 generations backK151051 Universa Soft Ureteral Stents and Stent SetsCook Incorporated · 2016 · Recalled
  6. 1 generation backK161236 Universa Firm Ureteral Stents and Stent SetsCook Incorporated · 2017 · Recalled
  7. This deviceK251890 Disposable Ureteral StentsZhejiang Chuangxiang Medical Technology Co., Ltd. · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K903345Bard (R) Lubricious - Coated Ureteral Stent SutureC.R. Bard, Inc.1991—
−5K983498Bard Inlay Lubricious Double Pigtail Ureteral Stent with Suture (Hereinafter…C.R. Bard, Inc.19982
−4K022447Bard ER Ureteral Stent with SutureC.R. Bard, Inc.2003—
−3K043193Bard Inlayoptima Ureteral Stent with SutureC.R. Bard, Inc.20046
−2K151051Universa Soft Ureteral Stents and Stent SetsCook Incorporated20162
−1K161236Universa Firm Ureteral Stents and Stent SetsCook Incorporated20171
0 (this device)K251890Disposable Ureteral StentsZhejiang Chuangxiang Medical Technology Co., Ltd.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
199610
FIG. 1 — Lineage of K251890, 1991–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in FAD? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new FAD device

  1. #1 K243830 Disposable ureteral stentscore 11.1 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K161236Universa Firm Ureteral Stents and Stent Sets
Summary page 5
…stroenterology/Urology Product Code: FAD III. Predicative and Reference Devices Predicate Device: 510(k) Number: K161236 510(k) Holder: Cook Incorporated Trade Name of Device: UniversaTM Firm Ureteral Stents and…
Cook Incorporated20171
†K243830Disposable ureteral stentShenzhen Trious Medical Technology Co., Ltd.2025—

Also cleared against K161236: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 35 years and passes through 3 companies; a new generation was cleared every 7.6 years on median.
  • 5 of the 8 ancestors have a recall of any class.
  • 2 other devices also cite its predicate K161236.

How does its category compare?

All FAD devices

FAD Stent, Ureteral: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · FAD

4in 2025

2007: 12008: 12010: 12014: 12016: 42017: 82018: 92019: 52020: 12021: 22022: 52024: 12025: 42026 (partial year): 1
2007high 9 (2018) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FAD

186in 2025

2016: 143 days median2017: 266 days median2018: 258 days median2019: 263 days median2022: 143 days median2025: 186 days median
2007high 266 (2017) · low 143 (2016)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FAD

4in 2025

2007: 12008: 222009: 22010: 12016: 42019: 62020: 22021: 12022: 92025: 4
2007high 22 (2008) · low 0 (2011)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · FAD

634in 2025

2007: 432008: 762009: 1232010: 782011: 952012: 1312013: 822014: 782015: 1302016: 1822017: 2652018: 2772019: 2612020: 3522021: 5312022: 5592023: 6912024: 6032025: 634
2007high 691 (2023) · low 43 (2007)2025

MAUDE reports naming product code FAD, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071—143
20081—2276
20090—2123
20101—178
20110—095
20120—0131
20130—082
20141—078
20150—0130
201641434182
201782660265
201892580277
201952636261
20201—2352
20212—1531
202251439559
20230—0691
20241—0603
202541864634
20261—0—

What is it indicated for?

The Disposable Ureteral Stents are used for temporary internal drainage from the ureteropelvic junction to the bladder. Ureteral stents have been used to relieve obstruction in a variety of benign, malignant and post-traumatic conditions. The stents are placed using endoscopic technique. The indwelling time should not exceed 30 days.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K251890: Disposable Ureteral Stents.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K251890

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026