510(k) Report

510(k) · Cleared

Cleared

Cooltouch; Cooltouch II; and Cooltouch CT3 ND:Yag Laser System

K040131510(k) TraditionalCleared Apr 20, 200490-day reviewClass II21 CFR 878.4810

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

New Star Lasers, Inc. · GEX Powered Laser Surgical Instrument

Cleared on Apr 20, 2004 as substantially equivalent to K030834 (Candela Corp., 2003) after a 90-day review. Its family tree reaches back 4 generations to 2000. 569 later devices descend from it.

Decided
Apr 20, 2004
Review
90 days
Class
Class II
Product code
GEX
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K002421 (2000). 5 ancestors in all. 569 later devices descend from it, 5 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2001: 1 other ancestor2009: 8 descendants cleared2008: 16 descendants cleared2010: 17 descendants cleared2004: 1 descendant cleared2005: 1 descendant cleared2007: 8 descendants cleared2006: 3 descendants cleared2017: 27 descendants cleared2020: 35 descendants cleared2011: 16 descendants cleared2022: 47 descendants cleared2021: 30 descendants cleared2015: 23 descendants cleared2014: 23 descendants cleared2012: 16 descendants cleared2018: 26 descendants cleared2013: 16 descendants cleared2016: 35 descendants cleared2023: 35 descendants cleared2019: 18 descendants cleared2024: 63 descendants cleared2025: 65 descendants cleared2026: 40 descendants clearedK002421 · Candela Mid IR Diode Laser System · Candela Corp. · 2000K013825 · Candela Smoothbeam Laser System · Candela Corp. · 2002 · recalledK022884 · Candela Smoothbeam Laser System · Candela Corp. · 2003 · recalledK030834 · Candela Smoothbeam Laser System · Candela Corp. · 2003 · recalled200020052010201520202025
Other ancestors, by generationDescendants, by generation 4 generations back: 1 other ancestor 1 generation forward: 5 descendants2 generations forward: 25 descendants3 generations forward: 62 descendants4 generations forward: 88 descendants5 generations forward: 90 descendants6 generations forward: 96 descendants7 generations forward: 81 descendants8 generations forward: 58 descendants9 generations forward: 39 descendants10 generations forward: 15 descendants11 generations forward: 9 descendants12 generations forward: 1 descendant K030834 · Candela Smoothbeam Laser System · Candela Corp. · 2003 · recalledK022884 · Candela Smoothbeam Laser System · Candela Corp. · 2003 · recalledK013825 · Candela Smoothbeam Laser System · Candela Corp. · 2002 · recalledK002421 · Candela Mid IR Diode Laser System · Candela Corp. · 20000+5+10
  1. Root · 4 generations backK002421 Candela Mid IR Diode Laser SystemCandela Corp. · 2000
  2. 3 generations backK013825 Candela Smoothbeam Laser SystemCandela Corp. · 2002 · Recalled
  3. 2 generations backK022884 Candela Smoothbeam Laser SystemCandela Corp. · 2003 · Recalled
  4. 1 generation backK030834 Candela Smoothbeam Laser SystemCandela Corp. · 2003 · Recalled
  5. This deviceK040131 Cooltouch; Cooltouch II; and Cooltouch CT3 ND:Yag Laser SystemNew Star Lasers, Inc. · 2004
  6. Descendant · cites it directly · 517 of its ownK042000 Modified MSQ Family of Lovely Light/Laser SystemsMsq (M2), Ltd. · 2004
  7. Descendant · 2 generations on · 266 of its ownK072564 Alma Lasers Harmony XL Multi-Application PlatformAlma Lasers, Ltd. · 2008
  8. Descendant · 2 generations on · 221 of its ownK060033 Profile Multi-Platform SystemSciton, Inc · 2006
  9. Descendant · 3 generations on · 202 of its ownK073063 15W Ceralas D 1470NM Diode LaserBiolitec, Inc. · 2008
  10. Descendant · 3 generations on · 198 of its ownK083899 Revlite Q-Switched ND:Yag Laser SystemHoya Conbio, Inc. · 2009

Showing 5 of 569 descendants. See all descendants

Descendants cleared per year

2004: 12005: 12006: 32007: 82008: 162009: 82010: 172011: 162012: 162013: 162014: 232015: 232016: 352017: 272018: 262019: 182020: 352021: 302022: 472023: 352024: 632025: 652026: 40
2004high 65 (2025) · low 1 (2004)2026

Most influential descendants

Showing 5 of 569 · See all
  • K042000Modified MSQ Family of Lovely Light/Laser SystemsMsq (M2), Ltd. · 2004 · cites it directly517descendants
  • K072564Alma Lasers Harmony XL Multi-Application PlatformAlma Lasers, Ltd. · 2008 · 2 generations on266descendants
  • K060033Profile Multi-Platform SystemSciton, Inc · 2006 · 2 generations on221descendants
  • K07306315W Ceralas D 1470NM Diode LaserBiolitec, Inc. · 2008 · 3 generations on202descendants
  • K083899Revlite Q-Switched ND:Yag Laser SystemHoya Conbio, Inc. · 2009 · 3 generations on198descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K002421Candela Mid IR Diode Laser SystemCandela Corp.2000—
−3K013825Candela Smoothbeam Laser SystemCandela Corp.20021
−2K022884Candela Smoothbeam Laser SystemCandela Corp.20031
−1K030834Candela Smoothbeam Laser SystemCandela Corp.20031
0 (this device)K040131Cooltouch; Cooltouch II; and Cooltouch CT3 ND:Yag Laser SystemNew Star Lasers, Inc.2004—
+1K042000Modified MSQ Family of Lovely Light/Laser SystemsMsq (M2), Ltd.2004—
+2K072564Alma Lasers Harmony XL Multi-Application PlatformAlma Lasers, Ltd.2008—
+2K060033Profile Multi-Platform SystemSciton, Inc2006—
+3K07306315W Ceralas D 1470NM Diode LaserBiolitec, Inc.2008—
+3K083899Revlite Q-Switched ND:Yag Laser SystemHoya Conbio, Inc.2009—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
200510
200630
200780
2008160
200980
2010170
2011160
2012160
2013160
2014230
2015230
2016350
2017270
2018260
2019180
2020350
2021300
2022470
2023350
2024630
2025650
2026400
FIG. 1 — Lineage of K040131, 2000–2026Source: 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 GEX? 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 GEX device

  1. #1 K222064 The Alma Soprano Titaniumscore 38.1 · 24 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
*K030834Candela Smoothbeam Laser System
Summary page 1
…79-GEX, 21 CFR 878-4810 Legally Marketed Predicate Device: Candela SmoothbeamTM Laser System K030834 Treatment of mild to moderate inflammatory acne vulgaris. Description of the CoolTouc…
Candela Corp.20031

Also cleared against K030834: 1 other device →

What descends from it? (569)

See all 569

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

NumberDeviceApplicantDecidedDescendants
K042000Modified MSQ Family of Lovely Light/Laser SystemsMsq (M2), Ltd.2004517
K070355Fotona Fidelis Iii ER:Yag/ND:Yag Laser System FamilyFotona D.D.2008194
K083889Fotona QX ND:Yag/KTP Laser System FamilyFotona D.D.2009166
K093162Fidelis Plus Iii D, at Fidelis D, Powerlase at D / Fidelis Plus Iii, at Fidelis…Fotona D.D.201083
K090126Fotona XP ND: Yag Laser System Family, Fotona XP, XP-2 Focus, Fotona XP Changer,Model…Fotona D.D.200980

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 4 years and passes through 2 companies; a new generation was cleared every 11 months on median.
  • 3 of the 5 ancestors have a recall of any class.
  • Of its descendants, K042000 (Msq (M2), Ltd., 2004) has gone furthest, with 517 descendants of its own.
  • 1 other device also cites its predicate K030834.

How does its category compare?

All GEX devices

GEX Powered Laser Surgical Instrument: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GEX

83in 2025

2007: 732008: 1072009: 692010: 502011: 412012: 452013: 462014: 612015: 472016: 512017: 672018: 512019: 412020: 522021: 532022: 602023: 522024: 822025: 832026 (partial year): 57
2007high 107 (2008) · low 41 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GEX

90in 2025

2007: 79 days median2008: 86 days median2009: 100 days median2010: 96 days median2011: 83 days median2012: 118 days median2013: 144 days median2014: 147 days median2015: 112 days median2016: 114 days median2017: 90 days median2018: 78 days median2019: 88 days median2020: 90 days median2021: 123 days median2022: 152 days median2023: 87 days median2024: 90 days median2025: 90 days median2026 (partial year): 90 days median
2007high 152 (2022) · low 78 (2018)2026

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

Recalls per year · GEX

3in 2024

2007: 92008: 22010: 42011: 182012: 52013: 32014: 62016: 12017: 5, 1 Class I2018: 52019: 62020: 12023: 62024: 32026 (partial year): 2
2007high 18 (2011) · low 0 (2009)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · GEX

2,720in 2025

2007: 3422008: 2322009: 2092010: 1,7112011: 3,0242012: 2,0002013: 2,2362014: 2,0362015: 2,0992016: 2,5852017: 2,9772018: 3,5252019: 2,7092020: 2,1832021: 3,4652022: 2,2882023: 2,3372024: 2,1872025: 2,720
2007high 3,525 (2018) · low 209 (2009)2025

MAUDE reports naming product code GEX, 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
200773799342
2008107862232
2009691000209
2010509641,711
20114183183,024
20124511852,000
20134614432,236
20146114762,036
20154711202,099
20165111412,585
201767905 (1)2,977
2018517853,525
2019418862,709
2020529012,183
20215312303,465
20226015202,288
2023528762,337
2024829032,187
2025839002,720
202657902—

What is it indicated for?

The CoolTouch®, CoolTouch® II, and CoolTouch® CT3 ND:YAG Laser Systems are indicated for the treatment of mild to moderate inflammatory acne vulgaris.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K040131: Cooltouch; Cooltouch II; and Cooltouch CT3 ND:Yag Laser System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K040131

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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