510(k) Report

510(k) · Cleared

Cleared

Alma Lasers Modified Diode Laser Module with SHR Treatment Mode for Use with the Family of Soprano XL Multi-Application

K112031510(k) SpecialCleared Sep 13, 201160-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

Alma Lasers, Inc. · GEX Powered Laser Surgical Instrument

Cleared on Sep 13, 2011 as substantially equivalent to K102716 (Alma Lasers, Inc., 2010) and 1 other predicate after a 60-day review. Its family tree reaches back 10 generations to 1992. 118 later devices descend from it.

Decided
Sep 13, 2011
Review
60 days
Class
Class II
Product code
GEX
Recalls
None
Predicates
2

Its longest line of descent runs back 10 generations to K910422 (1992). 58 ancestors in all, the oldest K871179 (1987). 118 later devices descend from it, 7 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2009: 1 other ancestor2006: 1 other ancestor2005: 3 other ancestors2001: 5 other ancestors2000: 7 other ancestors2004: 1 other ancestor2003: 4 other ancestors2002: 5 other ancestors1998: 3 other ancestors1997: 5 other ancestors1996: 3 other ancestors1999: 3 other ancestors1995: 1 other ancestor1990: 1 other ancestor1989: 1 other ancestor1988: 1 other ancestor1987: 2 other ancestors1993: 1 other ancestor2016: 4 descendants cleared2018: 7 descendants cleared2013: 2 descendants cleared2014: 3 descendants cleared2026: 9 descendants cleared2025: 15 descendants cleared2015: 5 descendants cleared2017: 3 descendants cleared2022: 15 descendants cleared2019: 8 descendants cleared2020: 13 descendants cleared2023: 10 descendants cleared2021: 11 descendants cleared2024: 13 descendants clearedK910422 · Model RD-1200 Ruby Laser System · Spectrum Medical Technologies, Inc. · 1992K961279 · Sharplan Lasers, Inc. Ruby Laser System · Sharplan Lasers, Inc. · 1996K962446 · Sharplan Ruby Laser System · Sharplan Lasers, Inc. · 1997K974536 · Photoderm HR System · Esc Medical Systems, Ltd. · 1998K013366 · Prolite Pulsed Light System for the Removal of Unwanted Hair · Medical Bio Care Sweden AB · 2002K022568 · Prolite/Plasmalite MPX Pulsed Light System for Treatment of Unwanted Hair · Medical Bio Care Sweden AB · 2002K023954 · Altus Medical Coolglide Laser Systems and Accessories · Altus Medical, Inc. · 2003K042165 · Cutera Tabletop Aesthetic Product · Cutera, Inc. · 2004 · recalledK080318 · Alma Laser Nir Module · Alma Lasers, Ltd. · 2008K102716 · Modified Alma Lasers Family of Soprano XL Multi-Application Platmforms · Alma Lasers, Inc. · 20101990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 6 other ancestors3 generations back: 3 other ancestors4 generations back: 4 other ancestors5 generations back: 16 other ancestors6 generations back: 14 other ancestors7 generations back: 3 other ancestors8 generations back: 1 other ancestor 1 generation forward: 7 descendants2 generations forward: 19 descendants3 generations forward: 36 descendants4 generations forward: 30 descendants5 generations forward: 19 descendants6 generations forward: 6 descendants7 generations forward: 1 descendant K102716 · Modified Alma Lasers Family of Soprano XL Multi-Application Platmforms · Alma Lasers, Inc. · 2010K080318 · Alma Laser Nir Module · Alma Lasers, Ltd. · 2008K042165 · Cutera Tabletop Aesthetic Product · Cutera, Inc. · 2004 · recalledK023954 · Altus Medical Coolglide Laser Systems and Accessories · Altus Medical, Inc. · 2003K022568 · Prolite/Plasmalite MPX Pulsed Light System for Treatment of Unwanted Hair · Medical Bio Care Sweden AB · 2002K013366 · Prolite Pulsed Light System for the Removal of Unwanted Hair · Medical Bio Care Sweden AB · 2002K974536 · Photoderm HR System · Esc Medical Systems, Ltd. · 1998K962446 · Sharplan Ruby Laser System · Sharplan Lasers, Inc. · 1997K961279 · Sharplan Lasers, Inc. Ruby Laser System · Sharplan Lasers, Inc. · 1996K910422 · Model RD-1200 Ruby Laser System · Spectrum Medical Technologies, Inc. · 1992−10−50+5
  1. Root · 10 generations backK910422 Model RD-1200 Ruby Laser SystemSpectrum Medical Technologies, Inc. · 1992
  2. 6 generations between
  3. 3 generations backK042165 Cutera Tabletop Aesthetic ProductCutera, Inc. · 2004 · Recalled
  4. 2 generations backK080318 Alma Laser Nir ModuleAlma Lasers, Ltd. · 2008
  5. 1 generation backK102716 Modified Alma Lasers Family of Soprano XL Multi-Application PlatmformsAlma Lasers, Inc. · 2010
  6. This deviceK112031 Alma Lasers Modified Diode Laser Module with SHR Treatment Mode for…Alma Lasers, Inc. · 2011
  7. Descendant · cites it directly · 57 of its ownK140009 Soprano Ice Multi-Application & Multi-Technology PlatformAlma Lasers, Ltd. · 2014
  8. Descendant · cites it directly · 53 of its ownK123483 Diode LaserBeijing Syntech Laser CO., LTD. · 2013
  9. Descendant · 2 generations on · 48 of its ownK141973 Diode Laser Hair Removal SystemBeijing Anchorfree Technology Co., Ltd. · 2014
  10. Descendant · 2 generations on · 40 of its ownK162659 Diode Laser Hair Removal SystemShandong Huamei Technology Co., Ltd. · 2017
  11. Descendant · 2 generations on · 32 of its ownK143519 The MeDioStar NeXT FamilyAsclepion Laser Technologies GmbH · 2015
Show all 10 generations
  1. Root · 10 generations backK910422 Model RD-1200 Ruby Laser SystemSpectrum Medical Technologies, Inc. · 1992
  2. 9 generations backK961279 Sharplan Lasers, Inc. Ruby Laser SystemSharplan Lasers, Inc. · 1996
  3. 8 generations backK962446 Sharplan Ruby Laser SystemSharplan Lasers, Inc. · 1997
  4. 7 generations backK974536 Photoderm HR SystemEsc Medical Systems, Ltd. · 1998
  5. 6 generations backK013366 Prolite Pulsed Light System for the Removal of Unwanted HairMedical Bio Care Sweden AB · 2002
  6. 5 generations backK022568 Prolite/Plasmalite MPX Pulsed Light System for Treatment of Unwanted…Medical Bio Care Sweden AB · 2002
  7. 4 generations backK023954 Altus Medical Coolglide Laser Systems and AccessoriesAltus Medical, Inc. · 2003
  8. 3 generations backK042165 Cutera Tabletop Aesthetic ProductCutera, Inc. · 2004 · Recalled
  9. 2 generations backK080318 Alma Laser Nir ModuleAlma Lasers, Ltd. · 2008
  10. 1 generation backK102716 Modified Alma Lasers Family of Soprano XL Multi-Application PlatmformsAlma Lasers, Inc. · 2010
  11. This deviceK112031 Alma Lasers Modified Diode Laser Module with SHR Treatment Mode for…Alma Lasers, Inc. · 2011

Showing 5 of 118 descendants. See all descendants

Descendants cleared per year

2013: 22014: 32015: 52016: 42017: 32018: 72019: 82020: 132021: 112022: 152023: 102024: 132025: 152026: 9
2013high 15 (2022) · low 2 (2013)2026

Most influential descendants

Showing 5 of 118 · See all
  • K140009Soprano Ice Multi-Application & Multi-Technology PlatformAlma Lasers, Ltd. · 2014 · cites it directly57descendants
  • K123483Diode LaserBeijing Syntech Laser CO., LTD. · 2013 · cites it directly53descendants
  • K141973Diode Laser Hair Removal SystemBeijing Anchorfree Technology Co., Ltd. · 2014 · 2 generations on48descendants
  • K162659Diode Laser Hair Removal SystemShandong Huamei Technology Co., Ltd. · 2017 · 2 generations on40descendants
  • K143519The MeDioStar NeXT FamilyAsclepion Laser Technologies GmbH · 2015 · 2 generations on32descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K910422Model RD-1200 Ruby Laser SystemSpectrum Medical Technologies, Inc.1992—
−9K961279Sharplan Lasers, Inc. Ruby Laser SystemSharplan Lasers, Inc.1996—
−8K962446Sharplan Ruby Laser SystemSharplan Lasers, Inc.1997—
−7K974536Photoderm HR SystemEsc Medical Systems, Ltd.1998—
−6K013366Prolite Pulsed Light System for the Removal of Unwanted HairMedical Bio Care Sweden AB2002—
−5K022568Prolite/Plasmalite MPX Pulsed Light System for Treatment of Unwanted HairMedical Bio Care Sweden AB2002—
−4K023954Altus Medical Coolglide Laser Systems and AccessoriesAltus Medical, Inc.2003—
−3K042165Cutera Tabletop Aesthetic ProductCutera, Inc.20041
−2K080318Alma Laser Nir ModuleAlma Lasers, Ltd.2008—
−1K102716Modified Alma Lasers Family of Soprano XL Multi-Application PlatmformsAlma Lasers, Inc.2010—
0 (this device)K112031Alma Lasers Modified Diode Laser Module with SHR Treatment Mode for Use with…Alma Lasers, Inc.2011—
+1K140009Soprano Ice Multi-Application & Multi-Technology PlatformAlma Lasers, Ltd.2014—
+1K123483Diode LaserBeijing Syntech Laser CO., LTD.2013—
+2K141973Diode Laser Hair Removal SystemBeijing Anchorfree Technology Co., Ltd.2014—
+2K162659Diode Laser Hair Removal SystemShandong Huamei Technology Co., Ltd.2017—
+2K143519The MeDioStar NeXT FamilyAsclepion Laser Technologies GmbH2015—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198720
198810
198910
199010
199310
199510
199630
199750
199830
199930
200070
200150
200250
200340
200410
200530
200610
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201320
201430
201550
201640
201730
201870
201980
2020130
2021110
2022150
2023100
2024130
2025150
202690
FIG. 1 — Lineage of K112031, 1992–2026Source: 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? (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
*K102716Modified Alma Lasers Family of Soprano XL Multi-Application Platmforms
Summary page 1
…GEX 11I. Predicate Devices * Modified Alma Lasers Family of Soprano Multi -Application Platforms [Soprano XLTM, Soprano XLiTM] (K 102716) * Alma Lasers Soprano XL Multi-Application Platform (K083848) IV. Product Description The Alma…
Alma Lasers, Inc.2010—
*K083848Alma Lasers Soprano XL Multi-Application Platform
Summary page 1
…Family of Soprano Multi -Application Platforms [Soprano XLTM, Soprano XLiTM] (K 102716) * Alma Lasers Soprano XL Multi-Application Platform (K083848) IV. Product Description The Alma Lasers Modified Diode Laser Module with SHR Treatment Mode for use wit h…
Alma Lasers, Ltd.2009—

Also cleared against K102716: 3 other devices →

What descends from it? (118)

See all 118

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

NumberDeviceApplicantDecidedDescendants
K140009Soprano Ice Multi-Application & Multi-Technology PlatformAlma Lasers, Ltd.201457
K123483Diode LaserBeijing Syntech Laser CO., LTD.201353
K153718Spirit Hair Removal laser FamilyActive Optical Systems, Ltd.20167
K181019Diode Laser SystemGuangzhou Huafei Tongda Technology Co., Ltd.20186
K122567Joule 810/940/980 Multi-Platform SystemSciton, Inc20136
K253251Leaseir MHR Xcell (console) (MHR-100b); Handpiece: Dual (810-b and Blend-b); Handpiece…Leaseir Technologies, Slu20260
K131838Diode Laser for Hiar RemovalBeijing Honkon Technologies Co., Ltd.20140

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 8 companies; a new generation was cleared every 1.6 years on median.
  • 3 of the 58 ancestors have a recall of any class.
  • Of its descendants, K140009 (Alma Lasers, Ltd., 2014) has gone furthest, with 57 descendants of its own.
  • 3 other devices also cite its predicate K102716.

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. 2011, this device’s year, is highlighted.

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 Alma Lasers Family of Soprano XL Multi-Application Platforms is intended for use in

dermatologic and general surgical procedures.

The Alma Lasers Modified Diode Laser Module (used with the Alma Lasers Family of

Soprano XL Multi-Application Platforms):

* The HR Mode is intended for hair removal, permanent hair reduction.

* The SHR Mode is intended for hair removal, permanent hair reduction.

* The LaserBlanche Mode is intended for the treatment of benign vascular and pigmented

lesions.

The Alma Lasers Family of Soprano XL Multi-Application Platforms is intended for use on all

skin types (Fitzpatrick skin types I-VI), including tanned skin.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K112031: Alma Lasers Modified Diode Laser Module with SHR Treatment Mode for Use with the Family of Soprano XL Multi-Application.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K112031

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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