510(k) Report

510(k) · Cleared

Cleared

Enseal G2 Tissue Sealer, Straight Jaw, Enseal G2 Tissue Sealer, Curved Jaw, Enseal Trio Tissue Sealer, 3 MM Curved Jaw,

K131435510(k) TraditionalCleared Oct 3, 2013136-day reviewClass II21 CFR 878.4400

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 · GEI Electrosurgical, Cutting & Coagulation & Accessories

Cleared on Oct 3, 2013 as substantially equivalent to K113572 (Covidien, Formerly Valleylab, A Division of Tyco H, 2012) and 4 other predicates after a 136-day review. Its family tree reaches back 7 generations to 1994. 5 later devices descend from it.

Decided
Oct 3, 2013
Review
136 days
Class
Class II
Product code
GEI
Recalls
None
Predicates
5

Its longest line of descent runs back 7 generations to K932293 (1994). 20 ancestors in all. 5 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2012: 1 other ancestor2011: 2 other ancestors2007: 2 other ancestors2001: 2 other ancestors2003: 1 other ancestor1996: 1 other ancestor1995: 4 other ancestors2021: 2 descendants cleared2018: 1 descendant cleared2017: 1 descendant cleared2023: 1 descendant clearedK932293 · Cabot Medical Bipolar Cutting Forceps · Cabot Medical Corp. · 1994 · recalledK981916 · Ligasure Vessel Sealing System · Valleylab, Inc. · 1998K031133 · Surgrx Enseal Vessel Sealing and Hemostasis System Including the Enseal Controller Adapter, Enseal Open and Laparoscopis · Surgrx, Inc. · 2003×2: 2 generations cleared close together, K061526 (2006), K063097 (2006) K070896 · Enseal PTC Tissue Sealing Device · Surgrx, Inc. · 2007 · recalledK123141 · Enseal Trio Tissue Sealing Device · Ethicon Endo-Surgery, LLC · 20121990200020102020
  1. Root · 7 generations backK932293 Cabot Medical Bipolar Cutting ForcepsCabot Medical Corp. · 1994 · Recalled
  2. 6 generations backK981916 Ligasure Vessel Sealing SystemValleylab, Inc. · 1998
  3. 5 generations backK031133 Surgrx Enseal Vessel Sealing and Hemostasis System Including the…Surgrx, Inc. · 2003
  4. 4 generations backK061526 Enseal PTC Tissue Sealing DeviceSurgrx, Inc. · 2006
  5. 3 generations backK063097 Enseal PTC Tissue Sealing DeviceSurgrx, Inc. · 2006
  6. 2 generations backK070896 Enseal PTC Tissue Sealing DeviceSurgrx, Inc. · 2007 · Recalled
  7. 1 generation backK123141 Enseal Trio Tissue Sealing DeviceEthicon Endo-Surgery, LLC · 2012
  8. This deviceK131435 Enseal G2 Tissue Sealer, Straight Jaw, Enseal G2 Tissue Sealer…Ethicon Endo-Surgery, LLC · 2013
  9. Descendant · cites it directly · 1 of its ownK201696 ENSEAL X1 Tissue Sealer, Straight Jaw, 25 cm Shaft Length, ENSEAL X1…Ethicon Endo-Surgery, LLC · 2021
  10. Descendant · cites it directly · 1 of its ownK201066 ENSEAL X1 Tissue Sealer, Curved Jaw, 25 cm Shaft Length, ENSEAL X1…Ethicon Endo-Surgery, LLC · 2021
  11. Descendant · 2 generations on · 0 of its ownK230387 ENSEAL X1 Curved Tissue Sealers, 25 cm shaft length (NSLX125C)…Ethicon Endo-Surgery, LLC · 2023
  12. Descendant · cites it directly · 0 of its ownK180403 ENSEAL X1 Tissue Sealer, Curved Jaw, Articulating 37 cm Shaft…Ethicon Endo-Surgery, LLC · 2018
  13. Descendant · cites it directly · 0 of its ownK172580 ENSEAL X1 Tissue Sealer, Straight Jaw, 25 cm Shaft Length, ENSEAL X1…Ethicon Endo-Surgery, LLC · 2017 · Recalled

Most influential descendants

Showing 5 of 5 · See all
  • K201696ENSEAL X1 Tissue Sealer, Straight Jaw, 25 cm Shaft Length, ENSEAL X1 Tissue Sealer…Ethicon Endo-Surgery, LLC · 2021 · cites it directly1descendant
  • K201066ENSEAL X1 Tissue Sealer, Curved Jaw, 25 cm Shaft Length, ENSEAL X1 Tissue Sealer, Curved…Ethicon Endo-Surgery, LLC · 2021 · cites it directly1descendant
  • K230387ENSEAL X1 Curved Tissue Sealers, 25 cm shaft length (NSLX125C); ENSEAL X1 Curved Tissue…Ethicon Endo-Surgery, LLC · 2023 · 2 generations on0descendants
  • K180403ENSEAL X1 Tissue Sealer, Curved Jaw, Articulating 37 cm Shaft Length; ENSEAL X1 Tissue…Ethicon Endo-Surgery, LLC · 2018 · cites it directly0descendants
  • K172580ENSEAL X1 Tissue Sealer, Straight Jaw, 25 cm Shaft Length, ENSEAL X1 Tissue Sealer…Ethicon Endo-Surgery, LLC · 2017 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K932293Cabot Medical Bipolar Cutting ForcepsCabot Medical Corp.19943
−6K981916Ligasure Vessel Sealing SystemValleylab, Inc.1998—
−5K031133Surgrx Enseal Vessel Sealing and Hemostasis System Including the Enseal…Surgrx, Inc.2003—
−4K061526Enseal PTC Tissue Sealing DeviceSurgrx, Inc.2006—
−3K063097Enseal PTC Tissue Sealing DeviceSurgrx, Inc.2006—
−2K070896Enseal PTC Tissue Sealing DeviceSurgrx, Inc.20071
−1K123141Enseal Trio Tissue Sealing DeviceEthicon Endo-Surgery, LLC2012—
0 (this device)K131435Enseal G2 Tissue Sealer, Straight Jaw, Enseal G2 Tissue Sealer, Curved Jaw…Ethicon Endo-Surgery, LLC2013—
+1K201696ENSEAL X1 Tissue Sealer, Straight Jaw, 25 cm Shaft Length, ENSEAL X1 Tissue…Ethicon Endo-Surgery, LLC2021—
+1K201066ENSEAL X1 Tissue Sealer, Curved Jaw, 25 cm Shaft Length, ENSEAL X1 Tissue…Ethicon Endo-Surgery, LLC2021—
+2K230387ENSEAL X1 Curved Tissue Sealers, 25 cm shaft length (NSLX125C); ENSEAL X1…Ethicon Endo-Surgery, LLC2023—
+1K180403ENSEAL X1 Tissue Sealer, Curved Jaw, Articulating 37 cm Shaft Length; ENSEAL…Ethicon Endo-Surgery, LLC2018—
+1K172580ENSEAL X1 Tissue Sealer, Straight Jaw, 25 cm Shaft Length, ENSEAL X1 Tissue…Ethicon Endo-Surgery, LLC20173

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199540
199610
200120
200310
200720
201120
201210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
201810
202120
202310
FIG. 1 — Lineage of K131435, 1994–2023Source: 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 GEI? 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 GEI device

  1. #1 K231790 The InMode System with the Morpheus8 Applicatorsscore 32.7 · 21 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? (5)

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
*K113572Ligasure Curved, Small Jaw, Open Sealer/Divider
Summary page 1
…Electrocautery, Gynecologic and Accessories (21 CER 884.4120, Product Code HGt) Classification: Class 11 Predicate Devices: KI 113572: LigaSure T M Curved Small Jaw, Open Sealer/Divider LF1212 K072 177: ENSEAL® Round Tip Tissue Sealing…
Covidien, Formerly Valleylab, A Division of Tyco H2012—
*K072177Enseal Vessel Sealing and Hemostasis System
Summary page 1
…Code HGt) Classification: Class 11 Predicate Devices: KI 113572: LigaSure T M Curved Small Jaw, Open Sealer/Divider LF1212 K072 177: ENSEAL® Round Tip Tissue Sealing Devices K072493: ENSEAL® Round Tip Tissue Sealing Device (45 cm s…
Surgrx, Inc.20071
*K072493Enseal Tissue Sealing Device
Summary page 1
…KI 113572: LigaSure T M Curved Small Jaw, Open Sealer/Divider LF1212 K072 177: ENSEAL® Round Tip Tissue Sealing Devices K072493: ENSEAL® Round Tip Tissue Sealing Device (45 cm shaft length) K 123141:…
Surgrx, Inc.2007—
*K123141Enseal Trio Tissue Sealing Device
Summary page 1
…nd Tip Tissue Sealing Devices K072493: ENSEAL® Round Tip Tissue Sealing Device (45 cm shaft length) K 123141: ENSEAL® Trio Tissue Sealing Device K1 12033: ENSEAL® 02 Tissue Sealers Device Description:…
Ethicon Endo-Surgery, LLC2012—
*K112033Enseal G2 Tissus Sealers
Summary page 1
…L® Round Tip Tissue Sealing Device (45 cm shaft length) K 123141: ENSEAL® Trio Tissue Sealing Device K1 12033: ENSEAL® 02 Tissue Sealers Device Description: The Ethicon Endo-Surgery ENSEALO Tissue Sealers are sterile, bio…
Ethicon Endo-Sugery, LLC20115

Also cleared against K113572: 8 other devices →

What descends from it? (5)

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

NumberDeviceApplicantDecidedDescendants
K201696ENSEAL X1 Tissue Sealer, Straight Jaw, 25 cm Shaft Length, ENSEAL X1 Tissue Sealer…Ethicon Endo-Surgery, LLC20211
K201066ENSEAL X1 Tissue Sealer, Curved Jaw, 25 cm Shaft Length, ENSEAL X1 Tissue Sealer, Curved…Ethicon Endo-Surgery, LLC20211
K180403ENSEAL X1 Tissue Sealer, Curved Jaw, Articulating 37 cm Shaft Length; ENSEAL X1 Tissue…Ethicon Endo-Surgery, LLC20180
K172580ENSEAL X1 Tissue Sealer, Straight Jaw, 25 cm Shaft Length, ENSEAL X1 Tissue Sealer…Ethicon Endo-Surgery, LLC20170

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 19 years and passes through 4 companies; a new generation was cleared every 3.0 years on median.
  • 6 of the 20 ancestors have a recall of any class.
  • Of its descendants, K201696 (Ethicon Endo-Surgery, LLC, 2021) has gone furthest, with 1 descendant of its own.
  • 8 other devices also cite its predicate K113572.

How does its category compare?

All GEI devices

GEI Electrosurgical, Cutting & Coagulation & Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · GEI

52in 2025

2007: 502008: 612009: 422010: 462011: 352012: 392013: 482014: 492015: 472016: 642017: 522018: 472019: 482020: 592021: 462022: 552023: 652024: 592025: 522026 (partial year): 43
2007high 65 (2023) · low 35 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GEI

113in 2025

2007: 51 days median2008: 71 days median2009: 130 days median2010: 109 days median2011: 135 days median2012: 133 days median2013: 136 days median2014: 103 days median2015: 123 days median2016: 108 days median2017: 72 days median2018: 93 days median2019: 93 days median2020: 105 days median2021: 146 days median2022: 150 days median2023: 104 days median2024: 125 days median2025: 113 days median2026 (partial year): 183 days median
2007high 183 (2026) · low 51 (2007)2026

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

Recalls per year · GEI

4in 2025

2007: 212008: 192009: 272010: 512011: 322012: 302013: 132014: 32015: 42016: 32017: 22018: 62019: 52020: 12021: 62022: 492023: 27, 4 Class I2024: 22, 10 Class I2025: 42026 (partial year): 8
2007high 51 (2010) · low 1 (2020)2026

Class I (14 since 2007) Class II/III not classified

Adverse event reports per year · GEI

7,592in 2025

2007: 2,7952008: 2,5562009: 3,5912010: 3,3772011: 4,4632012: 5,2162013: 4,8972014: 4,9082015: 4,9362016: 5,6162017: 6,0732018: 6,5452019: 7,0672020: 6,4902021: 6,3542022: 6,1032023: 7,1762024: 7,8972025: 7,592
2007high 7,897 (2024) · low 2,556 (2008)2025

MAUDE reports naming product code GEI, 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
20075051212,795
20086171192,556
200942130273,591
201046109513,377
201135135324,463
201239133305,216
201348136134,897
20144910334,908
20154712344,936
20166410835,616
2017527226,073
2018479366,545
2019489357,067
20205910516,490
20214614666,354
202255150496,103
20236510427 (4)7,176
20245912522 (10)7,897
20255211347,592
2026431838—

What is it indicated for?

The ENSEAL® Tissue Scalers are bipolar electrosurgical instruments for use with an electrosurgical generator. They are intended for use during open or laparoscopic surgical procedures to cut and seal vessels and to cut, grasp and dissect tissue during surgery. Indications for use include open and laparoscopic general, gynecological, urologic. thoracic, plastic and reconstructive, and ENT surgical procedures or any procedure where vessel ligation (cutting…

Read the full statement (145 words)

The ENSEAL® Tissue Scalers are bipolar electrosurgical instruments for use with an electrosurgical generator. They are intended for use during open or laparoscopic surgical procedures to cut and seal vessels and to cut, grasp and dissect tissue during surgery.

Indications for use include open and laparoscopic general, gynecological, urologic. thoracic, plastic and reconstructive, and ENT surgical procedures or any procedure where vessel ligation (cutting and sealing), tissue grasping, dissection, and division of vessels, lymphatics and tissue bundles is performed (e.g. bowel resections, hysterectomies, gall bladder procedures, Nissen Fundoplication, adhesiolysis, and oopborectomies).

The devices can be used on vessels up to and including 7 mm and bundles as large as will fit in the jaws of the instruments.

The ENSEAL® Tissue Scalers have not been shown to be effective for tubal sterilization or tubal coagulation for sterilization procedures. Do not use this system for these procedures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K131435: Enseal G2 Tissue Sealer, Straight Jaw, Enseal G2 Tissue Sealer, Curved Jaw, Enseal Trio Tissue Sealer, 3 MM Curved Jaw,.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K131435

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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