510(k) Report

510(k) · Cleared

Cleared

ECHELON 3000 45mm Compact Stapler (ECH45C); Echelon 3000 45mm Standard Stapler (ECH45S); Echelon 3000 45mm Long Stapler (ECH45L); Echelon 3000 60mm Compact Stapler (ECH60C); Echelon 3000 60mm Standard Stapler (ECH60S); Echelon 3000 60mm Long Stapler (ECH60L)

K241629510(k) SpecialCleared Jul 3, 202427-day reviewClass II21 CFR 878.4740

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

Ethicon Endo-Surgery, LLC · GAG Stapler, Surgical

Cleared on Jul 3, 2024 as substantially equivalent to K213633 (Ethicon Endo-Surgery, LLC, 2022) after a 27-day review. Its family tree reaches back 8 generations to 2005. 3 of the 16 devices in its family, counting itself, have a Class I recall. 3 later devices descend from it.

Decided
Jul 3, 2024
Review
27 days
Class
Class II
Product code
GAG
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K051002 (2005). 12 ancestors in all. 3 later devices descend from it, 2 citing it directly. 3 of the 16 devices in this family, counting this one, have a Class I recall.

  1. Root · 8 generations backK051002 Endopath Endocutter 60 Endoscopic Linear CutterEthicon Endo-Surgery, Inc. · 2005 · Recalled
  2. 7 generations backK081146 Echelon Endoscopic Linear Cutters (Articulating and Straight)Ethicon Endo-Surgery, LLC · 2008 · Recalled (Class I)
  3. 6 generations backK112056 Echelon 60 Endoscopic Linear Cutter Reload, Black Model ECR60T…Ethicon Endo-Surgery, LLC · 2011 · Recalled
  4. 5 generations backK121600 Echelon 60 Endoscpic Linear Cutter Reload, WhiteEthicon Endo-Surgery, LLC · 2012
  5. 4 generations backK140560 Echelon Flex Powered Plus Articulating Endoscopic Linear Cutter…Ethicon Endo-Surgery, LLC · 2014 · Recalled (Class I)
  6. 3 generations backK160521 ECHELON FLEX 60 Powered Plus Compact Articulating Endoscopic Linear…Ethicon Endo-Surgery, LLC · 2016 · Recalled (Class I)
  7. 2 generations backK163454 ECHELON FLEX 45mm Powered Plus Articulating Endoscopic Linear…Ethicon Endo-Surgery, LLC · 2017 · Recalled
  8. 1 generation backK213633 ECHELON 3000 45mm Stapler, ECHELON 3000 60mm StaplerEthicon Endo-Surgery, LLC · 2022
  9. This deviceK241629 ECHELON 3000 45mm Compact Stapler (ECH45C); Echelon 3000 45mm…Ethicon Endo-Surgery, LLC · 2024
  10. Descendant · cites it directly · 1 of its ownK250835 ETHICON 4000 60mm Compact Stapler (EC3D60C); ETHICON 4000 60mm…Ethicon Endo-Surgery, LLC · 2025
  11. Descendant · cites it directly · 0 of its ownK253657 Tri-staple 2.0™ Reloads; Endo GIA™ Reloads with Tri-Staple™…Covidien (Part of Medtronic) · 2026
  12. Descendant · 2 generations on · 0 of its ownK252739 ETHICON™ 4000 45mm Compact Stapler (EC3DT45C); ETHICON™ 4000 45mm…Ethicon Endo-Surgery, LLC · 2025

Class I recalls in this family

Most influential descendants

Showing 3 of 3 · See all
  • K250835ETHICON 4000 60mm Compact Stapler (EC3D60C); ETHICON 4000 60mm Standard Stapler…Ethicon Endo-Surgery, LLC · 2025 · cites it directly1descendant
  • K253657Tri-staple 2.0™ Reloads; Endo GIA™ Reloads with Tri-Staple™ Technology; Endo GIA™ Gray…Covidien (Part of Medtronic) · 2026 · cites it directly0descendants
  • K252739ETHICON™ 4000 45mm Compact Stapler (EC3DT45C); ETHICON™ 4000 45mm Standard Stapler…Ethicon Endo-Surgery, LLC · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K051002Endopath Endocutter 60 Endoscopic Linear CutterEthicon Endo-Surgery, Inc.20051
−7K081146Echelon Endoscopic Linear Cutters (Articulating and Straight)Ethicon Endo-Surgery, LLC2008Class I
−6K112056Echelon 60 Endoscopic Linear Cutter Reload, Black Model ECR60T, Echelon 45…Ethicon Endo-Surgery, LLC20111
−5K121600Echelon 60 Endoscpic Linear Cutter Reload, WhiteEthicon Endo-Surgery, LLC2012—
−4K140560Echelon Flex Powered Plus Articulating Endoscopic Linear Cutter, 60MM…Ethicon Endo-Surgery, LLC2014Class I
−3K160521ECHELON FLEX 60 Powered Plus Compact Articulating Endoscopic Linear Cutter…Ethicon Endo-Surgery, LLC2016Class I
−2K163454ECHELON FLEX 45mm Powered Plus Articulating Endoscopic Linear Cutters, ECHELON…Ethicon Endo-Surgery, LLC20171
−1K213633ECHELON 3000 45mm Stapler, ECHELON 3000 60mm StaplerEthicon Endo-Surgery, LLC2022—
0 (this device)K241629ECHELON 3000 45mm Compact Stapler (ECH45C); Echelon 3000 45mm Standard Stapler…Ethicon Endo-Surgery, LLC2024—
+1K250835ETHICON 4000 60mm Compact Stapler (EC3D60C); ETHICON 4000 60mm Standard…Ethicon Endo-Surgery, LLC2025—
+1K253657Tri-staple 2.0™ Reloads; Endo GIA™ Reloads with Tri-Staple™ Technology; Endo…Covidien (Part of Medtronic)2026—
+2K252739ETHICON™ 4000 45mm Compact Stapler (EC3DT45C); ETHICON™ 4000 45mm Standard…Ethicon Endo-Surgery, LLC2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200710
201110
201320

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202520
202610
FIG. 1 — Lineage of K241629, 2005–2026Source: 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.

3 devices in this family have 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 GAG device

  1. #1 K253527 Tri-Staple™ 2.0 Black Circular Reload 21mm…score 13.4 · 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
*K213633ECHELON 3000 45mm Stapler, ECHELON 3000 60mm Stapler
Summary page 5
…Product Code K213633 ECHELON™ 3000 45mm Stapler GAG K213633 ECH…
Ethicon Endo-Surgery, LLC2022—

Also cleared against K213633: 1 other device →

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K250835ETHICON 4000 60mm Compact Stapler (EC3D60C); ETHICON 4000 60mm Standard Stapler…Ethicon Endo-Surgery, LLC20251
K253657Tri-staple 2.0™ Reloads; Endo GIA™ Reloads with Tri-Staple™ Technology; Endo GIA™ Gray…Covidien (Part of Medtronic)20260

Has anything in its family been recalled? (3 Class I)

No FDA recall names this device.

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.

  • K160521ECHELON FLEX 60 Powered Plus Compact Articulating Endoscopic Linear Cutter, 280mmEthicon Endo-Surgery, LLC · 2016 · 2 generations back · ◆ on the line of descent in FIG. 11 Class I recall
  • K140560Echelon Flex Powered Plus Articulating Endoscopic Linear Cutter, 60MM, Standard, Echelon Flex Powered Plus…Ethicon Endo-Surgery, LLC · 2014 · 2 generations back · ◆ on the line of descent in FIG. 12 Class I recalls
  • K081146Echelon Endoscopic Linear Cutters (Articulating and Straight)Ethicon Endo-Surgery, LLC · 2008 · 4 generations back · ◆ on the line of descent in FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 19 years and passes through 2 companies; a new generation was cleared every 2.2 years on median.
  • 7 of the 12 ancestors have a recall of any class; 3 have a Class I recall.
  • Of its descendants, K250835 (Ethicon Endo-Surgery, LLC, 2025) has gone furthest, with 1 descendant of its own.
  • 1 other device also cites its predicate K213633.

How does its category compare?

All GAG devices

GAG Stapler, Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · GAG

2in 2025

2022: 12023: 42024: 32025: 22026 (partial year): 1
2007high 4 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GAG

138in 2024

2023: 102 days median2024: 138 days median
2007high 138 (2024) · low 102 (2023)2026

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

Recalls per year · GAG

1in 2018

2010: 12012: 12018: 1
2007high 1 (2010) · low 0 (2007)2026

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

Adverse event reports per year · GAG

1,065in 2025

2007: 9192008: 3662009: 182010: 222011: 192012: 492013: 1352014: 3022015: 1442016: 752017: 962018: 812019: 702020: 472021: 532022: 502023: 1092024: 1,1262025: 1,065
2007high 1,126 (2024) · low 18 (2009)2025

MAUDE reports naming product code GAG, 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—0919
20080—0366
20090—018
20100—122
20110—019
20120—149
20130—0135
20140—0302
20150—0144
20160—075
20170—096
20180—181
20190—070
20200—047
20210—053
20221—050
202341020109
2024313801,126
20252—01,065
20261—0—

What is it indicated for?

The ECHELON™ 3000 and ECHELON ENDOPATH™ families of staplers and reloads are intended

for transection, resection, and/or creation of anastomoses. The instruments have applications in

multiple open or minimally invasive general, urologic, thoracic, and pediatric surgical procedures.

They can be used with staple line or tissue reinforcement materials. The instruments may also be

used for transection and resection of liver parenchyma (hepatic vasculature and biliary structures),

pancreas, kidney, and spleen.

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. “K241629: ECHELON 3000 45mm Compact Stapler (ECH45C); Echelon 3000 45mm Standard Stapler (ECH45S); Echelon 3000 45mm Long Stapler (ECH45L); Echelon 3000 60mm Compact Stapler (ECH60C); Echelon 3000 60mm Standard Stapler (ECH60S); Echelon 3000 60mm Long Stapler (ECH60L).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K241629

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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