510(k) Report

510(k) · Cleared

Recalled · Class II · 2019

Esophageal TTS Stent

K113551510(k) TraditionalCleared Feb 14, 201275-day reviewClass II21 CFR 878.3610Recalls 1

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

Taewoong Medical Co., Ltd. · ESW Prosthesis, Esophageal

Cleared on Feb 14, 2012 as substantially equivalent to K080782 (Taewoong Medical Co., Ltd., 2009) and 1 other predicate after a 75-day review. Its family tree reaches back 8 generations to 1992. 10 later devices descend from it. It has been recalled once.

Decided
Feb 14, 2012
Review
75 days
Class
Class II
Product code
ESW
Recalls
1
Predicates
2

Its longest line of descent runs back 8 generations to K923119 (1992). 29 ancestors in all, the oldest K911292 (1991). 10 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2009: 1 other ancestor2005: 1 other ancestor2004: 1 other ancestor2002: 2 other ancestors1994: 5 other ancestors2003: 1 other ancestor2000: 2 other ancestors1997: 1 other ancestor1996: 3 other ancestors2001: 1 other ancestor1998: 1 other ancestor1991: 2 other ancestors2022: 1 descendant cleared2021: 2 descendants cleared2013: 1 descendant cleared2020: 1 descendant cleared2018: 1 descendant cleared2024: 2 descendants cleared2025: 1 descendant cleared2026: 1 descendant clearedK923119 · Wallstent Esophageal Prothesis · Schneider U.S. Stent Div. · 1992K945494 · Wallstent (R) Tracheobronchial Endoprosthesis · Boston Scientific Scimed, Inc. · 1995 · recalledK961296 · Wallstent Tracheobronchial Endoprosthesis · Boston Scientific Scimed, Inc. · 1996 · recalledK964121 · Wallstent Tracheobronchial Endoprosthesis · Boston Scientific Scimed, Inc. · 1996 · recalled×2: 2 generations cleared close together, K980163 (1998), K982184 (1998) K012752 · Wallstent RX Biliary Endoprostheses, Models 6961-6972 Inclusive · Boston Scientific Corp · 2001 · recalledK073667 · Niti-S Biliary Stent · Taewoong Medical Co., Ltd. · 20081990200020102020
  1. Root · 8 generations backK923119 Wallstent Esophageal ProthesisSchneider U.S. Stent Div. · 1992
  2. 7 generations backK945494 Wallstent (R) Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc. · 1995 · Recalled
  3. 6 generations backK961296 Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc. · 1996 · Recalled
  4. 5 generations backK964121 Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc. · 1996 · Recalled
  5. 4 generations backK980163 Wallstent Tracheobronchial Endoprosthesis and Wallstent…Boston Scientific Scimed, Inc. · 1998 · Recalled
  6. 3 generations backK982184 Wallstent EndoprosthesisBoston Scientific Scimed, Inc. · 1998
  7. 2 generations backK012752 Wallstent RX Biliary Endoprostheses, Models 6961-6972 InclusiveBoston Scientific Corp · 2001 · Recalled
  8. 1 generation backK073667 Niti-S Biliary StentTaewoong Medical Co., Ltd. · 2008
  9. This deviceK113551 Esophageal TTS StentTaewoong Medical Co., Ltd. · 2012
  10. Descendant · cites it directly · 9 of its ownK123205 Esophageal TTS StentTaewoong Medical Co., Ltd. · 2013 · Recalled
  11. Descendant · cites it directly · 3 of its ownK211706 Esophageal TTS StentTaewoong Medical Co., Ltd. · 2021
  12. Descendant · 2 generations on · 3 of its ownK180144 Agile Esophageal Stent SystemBoston Scientific Corporation · 2018
  13. Descendant · cites it directly · 2 of its ownK221482 Esophageal TTS StentTaewoong Medical Co., Ltd. · 2022
  14. Descendant · 3 generations on · 2 of its ownK211960 Agile Esophageal OTW Stent SystemBoston Scientific Corporation · 2021

Showing 5 of 10 descendants. See all descendants

Descendants cleared per year

2013: 12018: 12020: 12021: 22022: 12024: 22025: 12026: 1
2013high 2 (2021) · low 0 (2014)2026

Most influential descendants

Showing 5 of 10 · See all
  • K123205Esophageal TTS StentTaewoong Medical Co., Ltd. · 2013 · cites it directly9descendants
  • K211706Esophageal TTS StentTaewoong Medical Co., Ltd. · 2021 · cites it directly3descendants
  • K180144Agile Esophageal Stent SystemBoston Scientific Corporation · 2018 · 2 generations on3descendants
  • K221482Esophageal TTS StentTaewoong Medical Co., Ltd. · 2022 · cites it directly2descendants
  • K211960Agile Esophageal OTW Stent SystemBoston Scientific Corporation · 2021 · 3 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K923119Wallstent Esophageal ProthesisSchneider U.S. Stent Div.1992—
−7K945494Wallstent (R) Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc.19951
−6K961296Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc.19961
−5K964121Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc.19961
−4K980163Wallstent Tracheobronchial Endoprosthesis and Wallstent Tracheobronchial…Boston Scientific Scimed, Inc.19981
−3K982184Wallstent EndoprosthesisBoston Scientific Scimed, Inc.1998—
−2K012752Wallstent RX Biliary Endoprostheses, Models 6961-6972 InclusiveBoston Scientific Corp20011
−1K073667Niti-S Biliary StentTaewoong Medical Co., Ltd.2008—
0 (this device)K113551Esophageal TTS StentTaewoong Medical Co., Ltd.2012—
+1K123205Esophageal TTS StentTaewoong Medical Co., Ltd.20131
+1K211706Esophageal TTS StentTaewoong Medical Co., Ltd.2021—
+2K180144Agile Esophageal Stent SystemBoston Scientific Corporation2018—
+1K221482Esophageal TTS StentTaewoong Medical Co., Ltd.2022—
+3K211960Agile Esophageal OTW Stent SystemBoston Scientific Corporation2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199120
199450
199630
199710
199810
200020
200110
200220
200310
200410
200510
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201310
201810
202010
202120
202210
202420
202510
202610
FIG. 1 — Lineage of K113551, 1992–2026Source: 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 ESW? 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 ESW device

  1. #1 K261978 WallFlex Esophageal Stent System;Agile…score 15.2 · 13 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? (2)

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
*K080782Niti-S Esophageal Stent
Summary page 1
…21 CFR 878.3610 Panel: General & Plastic Surgery Devices Product Code: ESW Predicate Devices: K080782 - Taewoong Niti-S Esophageal Stent K073667 - Taewoong Niti-S Biliary Stent Indication for Use: For…
Taewoong Medical Co., Ltd.20091
*K073667Niti-S Biliary Stent
Summary page 1
…al & Plastic Surgery Devices Product Code: ESW Predicate Devices: K080782 - Taewoong Niti-S Esophageal Stent K073667 - Taewoong Niti-S Biliary Stent Indication for Use: For use in esophageal strictures caused by intrinsic and/or extrinsic malign…
Taewoong Medical Co., Ltd.2008—

Also cleared against K080782: 4 other devices →

What descends from it? (10)

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

NumberDeviceApplicantDecidedDescendants
K123205Esophageal TTS StentTaewoong Medical Co., Ltd.20139
K211706Esophageal TTS StentTaewoong Medical Co., Ltd.20213
K221482Esophageal TTS StentTaewoong Medical Co., Ltd.20222

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

Recalls of this device

DateClassRecallRoot causeReason
Oct 18, 2019Class IIZ-1229-2020Error in labelingMisprinted IFUs shipped with esophageal stents

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 20 years and passes through 4 companies; a new generation was cleared every 2.5 years on median.
  • 10 of the 29 ancestors have a recall of any class.
  • Of its descendants, K123205 (Taewoong Medical Co., Ltd., 2013) has gone furthest, with 9 descendants of its own.
  • 4 other devices also cite its predicate K080782.

How does its category compare?

All ESW devices

ESW Prosthesis, Esophageal: FDA decisions, review times, recalls and adverse event reports over 20 years. 2012, this device’s year, is highlighted.

FDA decisions per year · ESW

3in 2025

2008: 52009: 32010: 32011: 12012: 22013: 22016: 12018: 22019: 12020: 12021: 42022: 12024: 42025: 32026 (partial year): 1
2007high 5 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ESW

90in 2025

2008: 99 days median2009: 35 days median2010: 206 days median2021: 139 days median2024: 130 days median2025: 90 days median
2007high 206 (2010) · low 35 (2009)2026

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

Recalls per year · ESW

25in 2010

2010: 25
2007high 25 (2010) · low 0 (2007)2026

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

Adverse event reports per year · ESW

120in 2025

2007: 882008: 1532009: 2392010: 2552011: 1402012: 1212013: 1452014: 1692015: 1752016: 1532017: 872018: 862019: 1672020: 1552021: 772022: 1092023: 1552024: 1662025: 120
2007high 255 (2010) · low 77 (2021)2025

MAUDE reports naming product code ESW, 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—088
20085990153
20093350239
2010320625255
20111—0140
20122—0121
20132—0145
20140—0169
20150—0175
20161—0153
20170—087
20182—086
20191—0167
20201—0155
20214139077
20221—0109
20230—0155
202441300166
20253900120
20261—0—

What is it indicated for?

For use in esophageal strictures caused by intrinsic and/or extrinsic malignant tumors.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K113551: Esophageal TTS Stent.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K113551

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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