510(k) Report

510(k) · Cleared

Cleared

LS Family of CO2 Lasers Including: LS-15 Laser System (15 Watt) and LS-25 Laser System (25 Watt)

K040563510(k) TraditionalCleared Oct 8, 2004219-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

Sandstone Medical Technologies, LLC · GEX Powered Laser Surgical Instrument

Cleared on Oct 8, 2004 as substantially equivalent to K030147 (Lumenis, Ltd., 2003) and 1 other predicate after a 219-day review. Its family tree reaches back 6 generations to 1994. 5 later devices descend from it.

Decided
Oct 8, 2004
Review
219 days
Class
Class II
Product code
GEX
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K936109 (1994). 26 ancestors in all, the oldest K822136 (1982). 5 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1995: 5 other ancestors1999: 2 other ancestors1998: 1 other ancestor1996: 3 other ancestors1994: 4 other ancestors1991: 1 other ancestor1990: 1 other ancestor1988: 1 other ancestor1986: 1 other ancestor1982: 1 other ancestor2010: 1 descendant cleared2008: 1 descendant cleared2011: 1 descendant cleared2015: 1 descendant cleared2016: 1 descendant clearedK936109 · Sharplan Model 1120 CO2 Surgical Laser · Sharplan Lasers, Inc. · 1994K960521 · Sharplan Lasers, Inc. Silktouch Flash Scanner · Sharplan Lasers, Inc. · 1996K963339 · Coherent Ultrapulse CO2 Surgical Lasers · Coherent Medical Group · 1997K974789 · Coherent Ultrapulse S Series CO2 Surgical Lasers Model C and L · Lumenis, Inc. · 1998×2: 2 generations cleared close together, K022060 (2002), K030147 (2003) 19801990200020102020
  1. Root · 6 generations backK936109 Sharplan Model 1120 CO2 Surgical LaserSharplan Lasers, Inc. · 1994
  2. 5 generations backK960521 Sharplan Lasers, Inc. Silktouch Flash ScannerSharplan Lasers, Inc. · 1996
  3. 4 generations backK963339 Coherent Ultrapulse CO2 Surgical LasersCoherent Medical Group · 1997
  4. 3 generations backK974789 Coherent Ultrapulse S Series CO2 Surgical Lasers Model C and LLumenis, Inc. · 1998
  5. 2 generations backK022060 Lumenis Ultrapulse Encore Carbon Dioxide Surgical Lasers and…Lumenis, Inc. · 2002
  6. 1 generation backK030147 Lumenis Family of Ultrapulse Surgitouch CO2 Surgical LasersLumenis, Ltd. · 2003
  7. This deviceK040563 LS Family of CO2 Lasers Including: LS-15 Laser System (15 Watt) and…Sandstone Medical Technologies, LLC · 2004
  8. Descendant · cites it directly · 3 of its ownK093793 LS-40 CO2 Laser System Model LS-40Sandstone Medical Technologies, LLC · 2010
  9. Descendant · 2 generations on · 2 of its ownK110897 Cortex CO2 / ER:Yag Laser SystemSandstone Medical Technologies, LLC · 2011
  10. Descendant · 3 generations on · 1 of its ownK150587 Cortex Laser SystemCynosure, Inc. Dba Ellman · 2015
  11. Descendant · 4 generations on · 0 of its ownK161356 Matrix LS-40 CO2 Laser SystemShanghai Wonderful Opto-Electrics Tech.Co.,Ltd · 2016
  12. Descendant · cites it directly · 0 of its ownK082101 LS Family of CO2 Lasers with Scanning HandpieceSandstone Medical Technologies, LLC · 2008

Most influential descendants

Showing 5 of 5 · See all
  • K093793LS-40 CO2 Laser System Model LS-40Sandstone Medical Technologies, LLC · 2010 · cites it directly3descendants
  • K110897Cortex CO2 / ER:Yag Laser SystemSandstone Medical Technologies, LLC · 2011 · 2 generations on2descendants
  • K150587Cortex Laser SystemCynosure, Inc. Dba Ellman · 2015 · 3 generations on1descendant
  • K161356Matrix LS-40 CO2 Laser SystemShanghai Wonderful Opto-Electrics Tech.Co.,Ltd · 2016 · 4 generations on0descendants
  • K082101LS Family of CO2 Lasers with Scanning HandpieceSandstone Medical Technologies, LLC · 2008 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K936109Sharplan Model 1120 CO2 Surgical LaserSharplan Lasers, Inc.1994—
−5K960521Sharplan Lasers, Inc. Silktouch Flash ScannerSharplan Lasers, Inc.1996—
−4K963339Coherent Ultrapulse CO2 Surgical LasersCoherent Medical Group1997—
−3K974789Coherent Ultrapulse S Series CO2 Surgical Lasers Model C and LLumenis, Inc.1998—
−2K022060Lumenis Ultrapulse Encore Carbon Dioxide Surgical Lasers and Delivery Device…Lumenis, Inc.2002—
−1K030147Lumenis Family of Ultrapulse Surgitouch CO2 Surgical LasersLumenis, Ltd.2003—
0 (this device)K040563LS Family of CO2 Lasers Including: LS-15 Laser System (15 Watt) and LS-25…Sandstone Medical Technologies, LLC2004—
+1K093793LS-40 CO2 Laser System Model LS-40Sandstone Medical Technologies, LLC2010—
+2K110897Cortex CO2 / ER:Yag Laser SystemSandstone Medical Technologies, LLC2011—
+3K150587Cortex Laser SystemCynosure, Inc. Dba Ellman2015—
+4K161356Matrix LS-40 CO2 Laser SystemShanghai Wonderful Opto-Electrics Tech.Co.,Ltd2016—
+1K082101LS Family of CO2 Lasers with Scanning HandpieceSandstone Medical Technologies, LLC2008—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198210
198610
198810
199010
199110
199440
199550
199630
199810
199920

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200810
201010
201110
201510
201610
FIG. 1 — Lineage of K040563, 1994–2016Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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? (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
*K030147Lumenis Family of Ultrapulse Surgitouch CO2 Surgical Lasers
Summary page 1
…ument, Surgical, Powered, laser 79-GEX, 21 CFR 87848 Legally Marketed Predicate Device: UltraPulse C02 Surgical Laser K030147 Luxar LX-20SP Surgical Laser K953074 Description of the LS Family of C02 The I…
Lumenis, Ltd.2003—
*K953074Modified Luxar LX-20 Family CO2 Laser System
Summary page 1
…X, 21 CFR 87848 Legally Marketed Predicate Device: UltraPulse C02 Surgical Laser K030147 Luxar LX-20SP Surgical Laser K953074 Description of the LS Family of C02 The IS Family of C02 Lasers are microprocessor-controlled Lasers:…
Luxar Corp.1995—

Also cleared against K030147: 14 other devices →

What descends from it? (5)

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

NumberDeviceApplicantDecidedDescendants
K093793LS-40 CO2 Laser System Model LS-40Sandstone Medical Technologies, LLC20103
K082101LS Family of CO2 Lasers with Scanning HandpieceSandstone Medical Technologies, LLC20080

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 10 years and passes through 5 companies; a new generation was cleared every 1.5 years on median.
  • None of the 26 ancestors has a recall.
  • Of its descendants, K093793 (Sandstone Medical Technologies, LLC, 2010) has gone furthest, with 3 descendants of its own.
  • 14 other devices also cite its predicate K030147.

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?

Coagulation, vaporization, ablation or cutting of soft tissue in dermatology and plastic surgery, general surgery, podiatry and otorhinolaryngology.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K040563: LS Family of CO2 Lasers Including: LS-15 Laser System (15 Watt) and LS-25 Laser System (25 Watt).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K040563

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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