510(k) Report

510(k) · Cleared

Cleared

Logic Laparoscopic Scissors

K063485510(k) TraditionalCleared Dec 1, 200614-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

Surgical Innovations Plc · GEI Electrosurgical, Cutting & Coagulation & Accessories

Cleared on Dec 1, 2006 as substantially equivalent to K040295 (Applied Medical Resources Corp., 2004) and 1 other predicate after a 14-day review. Its family tree reaches back 5 generations to 1993. 7 later devices descend from it.

Decided
Dec 1, 2006
Review
14 days
Class
Class II
Product code
GEI
Recalls
None
Predicates
2

Its longest line of descent runs back 5 generations to K932648 (1993). 11 ancestors in all, the oldest K903206 (1990). 7 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2004: 1 other ancestor1993: 1 other ancestor1990: 1 other ancestor1997: 1 other ancestor1994: 2 other ancestors2009: 1 descendant cleared2010: 1 descendant cleared2018: 1 descendant cleared2014: 1 descendant cleared2012: 1 descendant cleared2015: 1 descendant cleared2024: 1 descendant clearedK932648 · Quick Switch Laparoscopic Instruments · Microline Pentax, Inc. · 1993K962119 · RE-New Laparoscopic Instruments · Microline Pentax, Inc. · 1996 · recalledK970826 · Selecta-Tip Laparoscopic Scissors · Microline Pentax, Inc. · 1997K980758 · 3 MM Selec-Tip Laparoscopic Scissors · Microline Pentax, Inc. · 1998K014207 · Reposable Instrument System, Models MF001-MF083 · Aesculap, Inc. · 20021990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 2 other ancestors3 generations back: 1 other ancestor4 generations back: 2 other ancestors 1 generation forward: 2 descendants2 generations forward: 3 descendants3 generations forward: 1 descendant4 generations forward: 1 descendant K014207 · Reposable Instrument System, Models MF001-MF083 · Aesculap, Inc. · 2002K980758 · 3 MM Selec-Tip Laparoscopic Scissors · Microline Pentax, Inc. · 1998K970826 · Selecta-Tip Laparoscopic Scissors · Microline Pentax, Inc. · 1997K962119 · RE-New Laparoscopic Instruments · Microline Pentax, Inc. · 1996 · recalledK932648 · Quick Switch Laparoscopic Instruments · Microline Pentax, Inc. · 1993−50
  1. Root · 5 generations backK932648 Quick Switch Laparoscopic InstrumentsMicroline Pentax, Inc. · 1993
  2. 4 generations backK962119 RE-New Laparoscopic InstrumentsMicroline Pentax, Inc. · 1996 · Recalled
  3. 3 generations backK970826 Selecta-Tip Laparoscopic ScissorsMicroline Pentax, Inc. · 1997
  4. 2 generations backK980758 3 MM Selec-Tip Laparoscopic ScissorsMicroline Pentax, Inc. · 1998
  5. 1 generation backK014207 Reposable Instrument System, Models MF001-MF083Aesculap, Inc. · 2002
  6. This deviceK063485 Logic Laparoscopic ScissorsSurgical Innovations Plc · 2006
  7. Descendant · cites it directly · 4 of its ownK090583 Endoscopic Monopolar Scissors, Models Ems-235, Ems-165Apollo Endosurgery, Inc. · 2009
  8. Descendant · 2 generations on · 3 of its ownK141058 Ensizor Endoscopic ScissorsSlater Endoscopy, LLC · 2014
  9. Descendant · 3 generations on · 2 of its ownK150939 Ensizor Endoscopic ScissorsSlater Endoscopy, LLC · 2015
  10. Descendant · cites it directly · 1 of its ownK100109 Logiflex Laparoscopic Band Positioning DeviceSurgical Innovations Plc · 2010
  11. Descendant · 4 generations on · 0 of its ownK242923 SimpleSnip Endoscopic Suture Cutter (SC500160); SimpleSnip…Envision Endoscopy · 2024

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2009: 12010: 12012: 12014: 12015: 12018: 12024: 1
2009high 1 (2009) · low 0 (2011)2026

Most influential descendants

Showing 5 of 7 · See all
  • K090583Endoscopic Monopolar Scissors, Models Ems-235, Ems-165Apollo Endosurgery, Inc. · 2009 · cites it directly4descendants
  • K141058Ensizor Endoscopic ScissorsSlater Endoscopy, LLC · 2014 · 2 generations on3descendants
  • K150939Ensizor Endoscopic ScissorsSlater Endoscopy, LLC · 2015 · 3 generations on2descendants
  • K100109Logiflex Laparoscopic Band Positioning DeviceSurgical Innovations Plc · 2010 · cites it directly1descendant
  • K242923SimpleSnip Endoscopic Suture Cutter (SC500160); SimpleSnip Endoscopic Suture Cutter…Envision Endoscopy · 2024 · 4 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K932648Quick Switch Laparoscopic InstrumentsMicroline Pentax, Inc.1993—
−4K962119RE-New Laparoscopic InstrumentsMicroline Pentax, Inc.19962
−3K970826Selecta-Tip Laparoscopic ScissorsMicroline Pentax, Inc.1997—
−2K9807583 MM Selec-Tip Laparoscopic ScissorsMicroline Pentax, Inc.1998—
−1K014207Reposable Instrument System, Models MF001-MF083Aesculap, Inc.2002—
0 (this device)K063485Logic Laparoscopic ScissorsSurgical Innovations Plc2006—
+1K090583Endoscopic Monopolar Scissors, Models Ems-235, Ems-165Apollo Endosurgery, Inc.2009—
+2K141058Ensizor Endoscopic ScissorsSlater Endoscopy, LLC2014—
+3K150939Ensizor Endoscopic ScissorsSlater Endoscopy, LLC2015—
+1K100109Logiflex Laparoscopic Band Positioning DeviceSurgical Innovations Plc2010—
+4K242923SimpleSnip Endoscopic Suture Cutter (SC500160); SimpleSnip Endoscopic Suture…Envision Endoscopy2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199310
199420
199710
200410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
201010
201210
201410
201510
201810
202410
FIG. 1 — Lineage of K063485, 1993–2024Source: 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? (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
*K040295Applied Laparoscopic Monopolar Scissors
Summary page 1
…Applied Medical Laparoscopic Monopolar Scissors which is cleared to market under premarket notification K040295 Aesculap Resposable Instrument System which is cleared to market under…
Applied Medical Resources Corp.2004—
*K014207Reposable Instrument System, Models MF001-MF083
Summary page 1
…Aesculap Resposable Instrument System which is cleared to market under premarket notification K014207 INDICATIONS FOR USE: Surgical Innovations Resposable Laparoscopic Scissors are designed to cut, dissect, manipulate and/or caute…
Aesculap, Inc.2002—

Also cleared against K040295: 2 other devices →

What descends from it? (7)

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

NumberDeviceApplicantDecidedDescendants
K090583Endoscopic Monopolar Scissors, Models Ems-235, Ems-165Apollo Endosurgery, Inc.20094
K100109Logiflex Laparoscopic Band Positioning DeviceSurgical Innovations Plc20101

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 13 years and passes through 3 companies; a new generation was cleared every 2.8 years on median.
  • 1 of the 11 ancestors has a recall of any class.
  • Of its descendants, K090583 (Apollo Endosurgery, Inc., 2009) has gone furthest, with 4 descendants of its own.
  • 2 other devices also cite its predicate K040295.

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.

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?

Surgical Innovations Resposable Laparoscopic Scissors are designed to cut, dissect, manipulate and/or cauterize various tissue during endoscopic/laparoscopic, general, vascular gynaecological and thoracic surgical procedures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K063485: Logic Laparoscopic Scissors.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K063485

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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