510(k) Report

510(k) · Cleared

Cleared

Disposable Ureteral Access Sheath

K230748510(k) TraditionalCleared Aug 2, 2023138-day reviewClass II21 CFR 876.1500

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

Youcare Technology Co.,Ltd. (Wuhan) · FED Endoscopic Access Overtube, Gastroenterology-Urology

Cleared on Aug 2, 2023 as substantially equivalent to K151084 (Well Lead Medical Co., Ltd., 2016) after a 138-day review. Its family tree reaches back 4 generations to 2002. 5 later devices descend from it.

Decided
Aug 2, 2023
Review
138 days
Class
Class II
Product code
FED
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K022135 (2002). 7 ancestors in all. 5 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2013: 1 other ancestor2010: 1 other ancestor2003: 1 other ancestor2024: 1 descendant cleared2025: 3 descendants cleared2026: 1 descendant clearedK022135 · Ureteral Access Sheath Set (Uass) · Boston Scientific Corp · 2002K122649 · Navigator HD Ureteral Access Sheath Set · Boston Scientific Corp · 2012K140323 · Navigator HD Ureteral Access Sheath Sets · Boston Scientific · 2014K151084 · Well Lead Ureteral Access Sheath · Well Lead Medical Co., Ltd. · 2016200020052010201520202025
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 1 other ancestor4 generations back: 1 other ancestor 1 generation forward: 2 descendants2 generations forward: 3 descendants K151084 · Well Lead Ureteral Access Sheath · Well Lead Medical Co., Ltd. · 2016K140323 · Navigator HD Ureteral Access Sheath Sets · Boston Scientific · 2014K122649 · Navigator HD Ureteral Access Sheath Set · Boston Scientific Corp · 2012K022135 · Ureteral Access Sheath Set (Uass) · Boston Scientific Corp · 20020
  1. Root · 4 generations backK022135 Ureteral Access Sheath Set (Uass)Boston Scientific Corp · 2002
  2. 3 generations backK122649 Navigator HD Ureteral Access Sheath SetBoston Scientific Corp · 2012
  3. 2 generations backK140323 Navigator HD Ureteral Access Sheath SetsBoston Scientific · 2014
  4. 1 generation backK151084 Well Lead Ureteral Access SheathWell Lead Medical Co., Ltd. · 2016
  5. This deviceK230748 Disposable Ureteral Access SheathYoucare Technology Co.,Ltd. (Wuhan) · 2023
  6. Descendant · cites it directly · 2 of its ownK241181 Disposable Ureteral Guide SheathDongguan Zsr Biomedical Technology Company Limited · 2024
  7. Descendant · cites it directly · 1 of its ownK243710 Disposable ureteral access sheathShenzhen Trious Medical Technology Co., Ltd. · 2025
  8. Descendant · 2 generations on · 0 of its ownK260521 ClearEVAC Ureteral Aspirating Access Sheath…Zhuhai Pusen Medical Technology Co., Ltd. · 2026
  9. Descendant · 2 generations on · 0 of its ownK250695 Single-use Ureteral Access SheathShenzhen HugeMed Medical Technical Development Co., Ltd. · 2025
  10. Descendant · 2 generations on · 0 of its ownK250585 LumenaTM Ureteral Access SheathCathegenix (Xiamen) Co., Ltd. · 2025

Most influential descendants

Showing 5 of 5 · See all
  • K241181Disposable Ureteral Guide SheathDongguan Zsr Biomedical Technology Company Limited · 2024 · cites it directly2descendants
  • K243710Disposable ureteral access sheathShenzhen Trious Medical Technology Co., Ltd. · 2025 · cites it directly1descendant
  • K260521ClearEVAC Ureteral Aspirating Access Sheath (PUS-100-1040,PUS-100-1050…Zhuhai Pusen Medical Technology Co., Ltd. · 2026 · 2 generations on0descendants
  • K250695Single-use Ureteral Access SheathShenzhen HugeMed Medical Technical Development Co., Ltd. · 2025 · 2 generations on0descendants
  • K250585LumenaTM Ureteral Access SheathCathegenix (Xiamen) Co., Ltd. · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K022135Ureteral Access Sheath Set (Uass)Boston Scientific Corp2002—
−3K122649Navigator HD Ureteral Access Sheath SetBoston Scientific Corp2012—
−2K140323Navigator HD Ureteral Access Sheath SetsBoston Scientific2014—
−1K151084Well Lead Ureteral Access SheathWell Lead Medical Co., Ltd.2016—
0 (this device)K230748Disposable Ureteral Access SheathYoucare Technology Co.,Ltd. (Wuhan)2023—
+1K241181Disposable Ureteral Guide SheathDongguan Zsr Biomedical Technology Company Limited2024—
+1K243710Disposable ureteral access sheathShenzhen Trious Medical Technology Co., Ltd.2025—
+2K260521ClearEVAC Ureteral Aspirating Access Sheath (PUS-100-1040,PUS-100-1050…Zhuhai Pusen Medical Technology Co., Ltd.2026—
+2K250695Single-use Ureteral Access SheathShenzhen HugeMed Medical Technical Development Co., Ltd.2025—
+2K250585LumenaTM Ureteral Access SheathCathegenix (Xiamen) Co., Ltd.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200310
201010
201310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
202530
202610
FIG. 1 — Lineage of K230748, 2002–2026Source: 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 FED? 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 FED device

  1. #1 K241181 Disposable Ureteral Guide Sheathscore 15.0 · 5 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
*K151084Well Lead Ureteral Access Sheath
Summary page 4
…d-sheath-B Classification Name: Endoscope and accessories Regulation Number: 21 CFR§ 876.1500 Product Code: FED Device Classification: Class II 4. The Predicate Devices K151084 Well Lead Ureteral Access Sheath This predicate has not been subject to a design-related recall. No reference devices were used i…
Well Lead Medical Co., Ltd.2016—

Also cleared against K151084: 2 other devices →

What descends from it? (5)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K241181Disposable Ureteral Guide SheathDongguan Zsr Biomedical Technology Company Limited20242
K243710Disposable ureteral access sheathShenzhen Trious Medical Technology Co., Ltd.20251

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 21 years and passes through 4 companies; a new generation was cleared every 7.6 years on median.
  • None of the 7 ancestors has a recall.
  • Of its descendants, K241181 (Dongguan Zsr Biomedical Technology Company Limited, 2024) has gone furthest, with 2 descendants of its own.
  • 2 other devices also cite its predicate K151084.

How does its category compare?

All FED devices

FED Endoscopic Access Overtube, Gastroenterology-Urology: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · FED

11in 2025

2007: 12008: 12009: 42010: 32011: 12012: 42013: 22014: 42015: 22016: 52017: 12018: 42019: 52020: 42021: 32022: 12023: 32024: 62025: 112026 (partial year): 6
2007high 11 (2025) · low 1 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FED

120in 2025

2009: 90 days median2010: 90 days median2012: 82 days median2014: 123 days median2016: 126 days median2018: 122 days median2019: 94 days median2020: 117 days median2021: 189 days median2023: 138 days median2024: 98 days median2025: 120 days median2026 (partial year): 67 days median
2007high 189 (2021) · low 82 (2012)2026

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

Recalls per year · FED

4in 2024

2007: 12013: 32024: 4, 4 Class I
2007high 4 (2024) · low 0 (2008)2026

Class I (4 since 2007) Class II/III not classified

Adverse event reports per year · FED

115in 2025

2007: 142008: 182009: 192010: 192011: 202012: 352013: 252014: 342015: 352016: 292017: 322018: 342019: 302020: 332021: 552022: 362023: 532024: 642025: 115
2007high 115 (2025) · low 14 (2007)2025

MAUDE reports naming product code FED, 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—114
20081—018
2009490019
2010390019
20111—020
2012482035
20132—325
20144123034
20152—035
20165126029
20171—032
20184122034
2019594030
20204117033
20213189055
20221—036
20233138053
20246984 (4)64
2025111200115
20266670—

What is it indicated for?

The Disposable Ureteral Access Sheath is used to establish a conduit during endoscopic urological procedures facilitating the passage of endoscopes and other instruments into the urinary tract

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K230748: Disposable Ureteral Access Sheath.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K230748

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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