510(k) Report

510(k) · Decided

Decided

HANAROSTENT Benefit Biliary (NNN)

K202973510(k) TraditionalDecided May 11, 2021223-day reviewClass II21 CFR 876.5010

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

M.I.Tech Co., Ltd. · FGE Stents, Drains And Dilators For The Biliary Ducts

Cleared on May 11, 2021 as substantially equivalent to K111149 (M.I.Tech Co., Ltd., 2011) after a 223-day review. Its family tree reaches back 9 generations to 1992. 2 later devices descend from it.

Decided
May 11, 2021
Review
223 days
Class
Class II
Product code
FGE
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K923119 (1992). 25 ancestors in all, the oldest K911292 (1991). 2 later devices descend from it, 1 citing it directly.

  1. Root · 9 generations backK923119 Wallstent Esophageal ProthesisSchneider U.S. Stent Div. · 1992
  2. 5 generations between
  3. 3 generations backK012752 Wallstent RX Biliary Endoprostheses, Models 6961-6972 InclusiveBoston Scientific Corp · 2001 · Recalled
  4. 2 generations backK073667 Niti-S Biliary StentTaewoong Medical Co., Ltd. · 2008
  5. 1 generation backK111149 Hanarostent Biliary (NNN)M.I.Tech Co., Ltd. · 2011
  6. This deviceK202973 HANAROSTENT Benefit Biliary (NNN)M.I.Tech Co., Ltd. · 2021
  7. Descendant · cites it directly · 1 of its ownK221071 Niti-S Biliary Slim M StentTaewoong Medical Co., Ltd. · 2022
  8. Descendant · 2 generations on · 0 of its ownK251123 Niti-S Biliary Stent; Niti-S Biliary Slim M StentTaewoong Medical Co., Ltd. · 2025
Show all 9 generations
  1. Root · 9 generations backK923119 Wallstent Esophageal ProthesisSchneider U.S. Stent Div. · 1992
  2. 8 generations backK945494 Wallstent (R) Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc. · 1995 · Recalled
  3. 7 generations backK961296 Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc. · 1996 · Recalled
  4. 6 generations backK964121 Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc. · 1996 · Recalled
  5. 5 generations backK980163 Wallstent Tracheobronchial Endoprosthesis and Wallstent…Boston Scientific Scimed, Inc. · 1998 · Recalled
  6. 4 generations backK982184 Wallstent EndoprosthesisBoston Scientific Scimed, Inc. · 1998
  7. 3 generations backK012752 Wallstent RX Biliary Endoprostheses, Models 6961-6972 InclusiveBoston Scientific Corp · 2001 · Recalled
  8. 2 generations backK073667 Niti-S Biliary StentTaewoong Medical Co., Ltd. · 2008
  9. 1 generation backK111149 Hanarostent Biliary (NNN)M.I.Tech Co., Ltd. · 2011
  10. This deviceK202973 HANAROSTENT Benefit Biliary (NNN)M.I.Tech Co., Ltd. · 2021

Most influential descendants

Showing 2 of 2 · See all
  • K221071Niti-S Biliary Slim M StentTaewoong Medical Co., Ltd. · 2022 · cites it directly1descendant
  • K251123Niti-S Biliary Stent; Niti-S Biliary Slim M StentTaewoong Medical Co., Ltd. · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K923119Wallstent Esophageal ProthesisSchneider U.S. Stent Div.1992—
−8K945494Wallstent (R) Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc.19951
−7K961296Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc.19961
−6K964121Wallstent Tracheobronchial EndoprosthesisBoston Scientific Scimed, Inc.19961
−5K980163Wallstent Tracheobronchial Endoprosthesis and Wallstent Tracheobronchial…Boston Scientific Scimed, Inc.19981
−4K982184Wallstent EndoprosthesisBoston Scientific Scimed, Inc.1998—
−3K012752Wallstent RX Biliary Endoprostheses, Models 6961-6972 InclusiveBoston Scientific Corp20011
−2K073667Niti-S Biliary StentTaewoong Medical Co., Ltd.2008—
−1K111149Hanarostent Biliary (NNN)M.I.Tech Co., Ltd.2011—
0 (this device)K202973HANAROSTENT Benefit Biliary (NNN)M.I.Tech Co., Ltd.2021—
+1K221071Niti-S Biliary Slim M StentTaewoong Medical Co., Ltd.2022—
+2K251123Niti-S Biliary Stent; Niti-S Biliary Slim M StentTaewoong Medical Co., Ltd.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199120
199430
199630
199710
199810
200010
200110
200210
200310
200410
200510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
202510
FIG. 1 — Lineage of K202973, 1992–2025Source: 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 FGE? 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 FGE device

  1. #1 K240464 WallFlex Biliary RX Stent System; Epic Biliary…score 14.5 · 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? (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
*K111149Hanarostent Biliary (NNN)
Summary page 5
…radial force on the luminal surface of the biliary tract to establish patency. Predicate Device 510(k) Number: K111149 Applicant: M.I.Tech Co., Ltd. Trade Name:…
M.I.Tech Co., Ltd.2011—
†K163018Zilver 635 Biliary StentCook Ireland, Ltd.2016—
†K140630Wallflex Biliary RX Stent SystemBoston Scientific20141

Also cleared against K111149: 2 other devices →

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K221071Niti-S Biliary Slim M StentTaewoong Medical Co., Ltd.20221

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 29 years and passes through 5 companies; a new generation was cleared every 2.5 years on median.
  • 8 of the 25 ancestors have a recall of any class.
  • Of its descendants, K221071 (Taewoong Medical Co., Ltd., 2022) has gone furthest, with 1 descendant of its own.
  • 2 other devices also cite its predicate K111149.

How does its category compare?

All FGE devices

FGE Stents, Drains And Dilators For The Biliary Ducts: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · FGE

7in 2025

2007: 42008: 112009: 72010: 92011: 92012: 82013: 52014: 82015: 82016: 42017: 92018: 72019: 22020: 42021: 12022: 62023: 62024: 62025: 72026 (partial year): 8
2007high 11 (2008) · low 1 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FGE

257in 2025

2007: 316 days median2008: 214 days median2009: 160 days median2010: 81 days median2011: 114 days median2012: 96 days median2013: 161 days median2014: 156 days median2015: 79 days median2016: 49 days median2017: 59 days median2018: 215 days median2020: 121 days median2022: 101 days median2023: 199 days median2024: 188 days median2025: 257 days median2026 (partial year): 153 days median
2007high 316 (2007) · low 49 (2016)2026

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

Recalls per year · FGE

1in 2024

2007: 542008: 932009: 182010: 322011: 22012: 42013: 32017: 12018: 432019: 132020: 12021: 272022: 212023: 192024: 12026 (partial year): 11
2007high 93 (2008) · low 0 (2014)2026

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

Adverse event reports per year · FGE

1,923in 2025

2007: 1,0062008: 1,4652009: 1,6552010: 1,4342011: 1,3212012: 1,1832013: 1,0602014: 1,2702015: 1,5432016: 1,4532017: 1,5152018: 1,6812019: 1,8962020: 2,1822021: 2,2972022: 1,7492023: 1,6152024: 1,9482025: 1,923
2007high 2,297 (2021) · low 1,006 (2007)2025

MAUDE reports naming product code FGE, 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
20074316541,006
200811214931,465
20097160181,655
2010981321,434
2011911421,321
201289641,183
2013516131,060
2014815601,270
201587901,543
201644901,453
201795911,515
20187215431,681
20192—131,896
2020412112,182
20211—272,297
20226101211,749
20236199191,615
2024618811,948
2025725701,923
2026815311—

What is it indicated for?

The HANAROSTENT® Benefit™ Biliary (NNN) is indicated for the palliation of malignant strictures in the biliary tree.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K202973: HANAROSTENT Benefit Biliary (NNN).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K202973

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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