510(k) Report

510(k) · Cleared

Recalled · Class II · 2022

Flexible Video-Uretero-Renoscope System

K141250510(k) SpecialCleared Jun 11, 201428-day reviewClass II21 CFR 876.1500Recalls 2

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

KARL STORZ Endoscopy-America, Inc. · FGB Ureteroscope And Accessories, Flexible/Rigid

Cleared on Jun 11, 2014 as substantially equivalent to K131369 (KARL STORZ Endoscopy-America, Inc., 2013) after a 28-day review. Its family tree reaches back 8 generations to 1993. 1 of the 36 devices in its family, counting itself, has a Class I recall. 11 later devices descend from it. It has been recalled 2 times.

Decided
Jun 11, 2014
Review
28 days
Class
Class II
Product code
FGB
Recalls
2
Predicates
1

Its longest line of descent runs back 8 generations to K931154 (1993). 24 ancestors in all, the oldest K843084 (1985). 11 later devices descend from it, 4 citing it directly. 1 of the 36 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2001: 4 other ancestors2003: 1 other ancestor1997: 2 other ancestors1995: 2 other ancestors1991: 2 other ancestors, 1 with a Class I recall12000: 1 other ancestor1993: 1 other ancestor1992: 1 other ancestor1985: 2 other ancestors2014: 1 descendant cleared2025: 2 descendants cleared2022: 2 descendants cleared2020: 1 descendant cleared2023: 2 descendants cleared2024: 1 descendant cleared2026: 2 descendants clearedK931154 · Evis 200 System · Olympus Corp. · 1993K963033 · BF 240/P240/IT240 Bronchovideoscope & Accessories · Olympus America, Inc. · 1996 · recalledK981543 · Olympus LF-TP and LF-DP Tracheal Intubation Fiberscopes, Accessories and Ancillary Equipment · The Olympus Optical Co. · 1998 · recalledK021074 · Visera Cystovideoscope Olympus Cyf Type V/VA · Olympus America, Inc. · 2002K030960 · Ecn Electronic Video Cystonephroscope · Acmi Corporation · 2003K042225 · Acmi Invisio Icn, Models Icn-0564 and Icn-0565 · Acmi Corporation · 2004K060269 · Acmi Dur-Digital Ureteroscope and Choledochoscope System · Acmi Corporation · 2006K131369 · Flexible Video-Uretero-Renoscope System · KARL STORZ Endoscopy-America, Inc. · 2013 · recalled1990200020102020
  1. Root · 8 generations backK931154 Evis 200 SystemOlympus Corp. · 1993
  2. 7 generations backK963033 BF 240/P240/IT240 Bronchovideoscope & AccessoriesOlympus America, Inc. · 1996 · Recalled
  3. 6 generations backK981543 Olympus LF-TP and LF-DP Tracheal Intubation Fiberscopes, Accessories…The Olympus Optical Co. · 1998 · Recalled
  4. 5 generations backK021074 Visera Cystovideoscope Olympus Cyf Type V/VAOlympus America, Inc. · 2002
  5. 4 generations backK030960 Ecn Electronic Video CystonephroscopeAcmi Corporation · 2003
  6. 3 generations backK042225 Acmi Invisio Icn, Models Icn-0564 and Icn-0565Acmi Corporation · 2004
  7. 2 generations backK060269 Acmi Dur-Digital Ureteroscope and Choledochoscope SystemAcmi Corporation · 2006
  8. 1 generation backK131369 Flexible Video-Uretero-Renoscope SystemKARL STORZ Endoscopy-America, Inc. · 2013 · Recalled
  9. This deviceK141250 Flexible Video-Uretero-Renoscope SystemKARL STORZ Endoscopy-America, Inc. · 2014
  10. Descendant · cites it directly · 7 of its ownK142556 Flexible Video-Uretero-Choledochoscope SystemKARL STORZ Endoscopy-America, Inc. · 2014
  11. Descendant · 2 generations on · 3 of its ownK200483 SpyGlass Discover Digital Catheter, SpyGlass Discover Digital…Boston Scientific Corporation · 2020
  12. Descendant · 3 generations on · 2 of its ownK221784 Single-use Video Pancreaticobiliary Scope, PB Digital ControllerMicro-Tech (Nanjing) Co., Ltd. · 2023
  13. Descendant · 2 generations on · 2 of its ownK211686 Flexible Video-Choledo-Cysto-Ureteroscope SystemShanghai SeeGen Photoelectric Technology Co., Ltd. · 2022
  14. Descendant · 4 generations on · 0 of its ownK252492 Visualized Access and Delivery Catheter; PB Digital ControllerMicro-Tech (Nanjing) Co., Ltd. · 2026

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2014: 12020: 12022: 22023: 22024: 12025: 22026: 2
2014high 2 (2022) · low 0 (2015)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 11 · See all
  • K142556Flexible Video-Uretero-Choledochoscope SystemKARL STORZ Endoscopy-America, Inc. · 2014 · cites it directly7descendants
  • K200483SpyGlass Discover Digital Catheter, SpyGlass Discover Digital ControllerBoston Scientific Corporation · 2020 · 2 generations on3descendants
  • K221784Single-use Video Pancreaticobiliary Scope, PB Digital ControllerMicro-Tech (Nanjing) Co., Ltd. · 2023 · 3 generations on2descendants
  • K211686Flexible Video-Choledo-Cysto-Ureteroscope SystemShanghai SeeGen Photoelectric Technology Co., Ltd. · 2022 · 2 generations on2descendants
  • K252492Visualized Access and Delivery Catheter; PB Digital ControllerMicro-Tech (Nanjing) Co., Ltd. · 2026 · 4 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K931154Evis 200 SystemOlympus Corp.1993—
−7K963033BF 240/P240/IT240 Bronchovideoscope & AccessoriesOlympus America, Inc.19966
−6K981543Olympus LF-TP and LF-DP Tracheal Intubation Fiberscopes, Accessories and…The Olympus Optical Co.19985
−5K021074Visera Cystovideoscope Olympus Cyf Type V/VAOlympus America, Inc.2002—
−4K030960Ecn Electronic Video CystonephroscopeAcmi Corporation2003—
−3K042225Acmi Invisio Icn, Models Icn-0564 and Icn-0565Acmi Corporation2004—
−2K060269Acmi Dur-Digital Ureteroscope and Choledochoscope SystemAcmi Corporation2006—
−1K131369Flexible Video-Uretero-Renoscope SystemKARL STORZ Endoscopy-America, Inc.20131
0 (this device)K141250Flexible Video-Uretero-Renoscope SystemKARL STORZ Endoscopy-America, Inc.2014—
+1K142556Flexible Video-Uretero-Choledochoscope SystemKARL STORZ Endoscopy-America, Inc.2014—
+2K200483SpyGlass Discover Digital Catheter, SpyGlass Discover Digital ControllerBoston Scientific Corporation2020—
+3K221784Single-use Video Pancreaticobiliary Scope, PB Digital ControllerMicro-Tech (Nanjing) Co., Ltd.2023—
+2K211686Flexible Video-Choledo-Cysto-Ureteroscope SystemShanghai SeeGen Photoelectric Technology Co., Ltd.2022—
+4K252492Visualized Access and Delivery Catheter; PB Digital ControllerMicro-Tech (Nanjing) Co., Ltd.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198520
199121
199210
199310
199520
199720
200010
200140
200310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201410
202010
202220
202320
202410
202520
202620
FIG. 1 — Lineage of K141250, 1993–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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.

1 device in this family has a Class I recall. 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 FGB device

  1. #1 K251951 Single-Use Video Flexible Ureterorenoscope…score 16.2 · 10 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

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
*K131369Flexible Video-Uretero-Renoscope System
Summary page 1
…FG B Regulation: 21 CFR part 876.1500 Predicate Device(s): KARL STORZ Flexible Videc-Uretero-Renoscope System, K13 1369 Device Description: The Flexible Video-Uretero-Renoscope System is used for visualization pu…
KARL STORZ Endoscopy-America, Inc.20131

Also cleared against K131369: 4 other devices →

What descends from it? (11)

See all 11

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

NumberDeviceApplicantDecidedDescendants
K142556Flexible Video-Uretero-Choledochoscope SystemKARL STORZ Endoscopy-America, Inc.20147
K243550KARL STORZ Flexible Video-Uretero-Renoscope (FLEX XC)Karl Storz SE & CO. KG20250
K243894F88 URE-SD/RD Flexible UreteroscopeSg Endoscopy Pte, Ltd.20250
K212458Flexible Video-Uretero-Renoscope SSU SystemKarl Storz Endoscopy America20220

Has anything in its family been recalled? (1 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Apr 1, 2022Class IIZ-1070-2022Under Investigation by firmFailure to achieve the expected six-log reduction in microorganisms following the disinfection process.
Apr 1, 2022Class IIZ-1069-2022Under Investigation by firmFailure to achieve the expected six-log reduction in microorganisms following the disinfection process.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K912120Urf-P2 Ureterorenofiberscope/CholedochofiberscopeOlympus Corp. · 1991 · 6 generations back · ◆ in the 1991 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 21 years and passes through 5 companies; a new generation was cleared every 1.7 years on median.
  • 8 of the 24 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K142556 (KARL STORZ Endoscopy-America, Inc., 2014) has gone furthest, with 7 descendants of its own.
  • 4 other devices also cite its predicate K131369.

How does its category compare?

All FGB devices

FGB Ureteroscope And Accessories, Flexible/Rigid: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · FGB

17in 2025

2012: 22013: 12014: 22015: 12017: 22018: 42019: 22020: 22021: 32022: 52023: 82024: 162025: 172026 (partial year): 9
2007high 17 (2025) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FGB

134in 2025

2018: 191 days median2021: 191 days median2022: 205 days median2023: 183 days median2024: 217 days median2025: 134 days median2026 (partial year): 140 days median
2007high 217 (2024) · low 134 (2025)2026

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

Recalls per year · FGB

15in 2024

2022: 42023: 12024: 152026 (partial year): 1
2007high 15 (2024) · low 0 (2007)2026

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

Adverse event reports per year · FGB

1,307in 2025

2007: 62008: 72009: 42010: 202011: 172012: 112013: 82014: 122015: 162016: 352017: 1422018: 1182019: 2072020: 4022021: 3252022: 4552023: 4582024: 5722025: 1,307
2007high 1,307 (2025) · low 4 (2009)2025

MAUDE reports naming product code FGB, 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
20070—06
20080—07
20090—04
20100—020
20110—017
20122—011
20131—08
20142—012
20151—016
20160—035
20172—0142
201841910118
20192—0207
20202—0402
202131910325
202252054455
202381831458
20241621715572
20251713401,307
202691401—

What is it indicated for?

The KARL STORZ Flexible Video-Uretero-Renoscope System Is Indicated for endoscopic examination In the urinary tract and can be used to examine the Interior of the kidney, and using additional accessories, to perform various diagnostic and therapeutic procedures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K141250: Flexible Video-Uretero-Renoscope System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K141250

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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