510(k) Report

510(k) · Cleared

Cleared

Tria Acne Treatment System, Model Ats-1 Otc

K090312510(k) TraditionalCleared Jan 5, 2010333-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

Tria Beauty, Inc. · GEX Powered Laser Surgical Instrument

Cleared on Jan 5, 2010 as substantially equivalent to K060567 (Spectragenics, Inc., 2006) and 3 other predicates after a 333-day review. Its family tree reaches back 8 generations to 1992. 1 later device descends from it.

Decided
Jan 5, 2010
Review
333 days
Class
Class II
Product code
GEX
Recalls
None
Predicates
4

Its longest line of descent runs back 8 generations to K910422 (1992). 66 ancestors in all, the oldest K892514 (1990). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2006: 1 other ancestor2005: 2 other ancestors2007: 1 other ancestor2004: 2 other ancestors2003: 4 other ancestors2002: 1 other ancestor1998: 5 other ancestors2001: 2 other ancestors2000: 3 other ancestors1999: 3 other ancestors1996: 7 other ancestors1995: 6 other ancestors1997: 6 other ancestors1994: 7 other ancestors1993: 3 other ancestors1991: 3 other ancestors1990: 1 other ancestor2016: 1 descendant 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. · 1998K991935 · Epilight Hair Removal System, Photoderm HR System · Esc Medical Systems, Ltd. · 2000K020839 · Quantum, Models SR, HR, DL; Vasculight, Models SR, HR, VS, VX, DL · Lumenis, Inc. · 2002K041086 · Palomar Starlux Pulsed Light System · Palomar Medical Products, Inc. · 2005K060567 · Spectragenics Ats-1 · Spectragenics, Inc. · 20061990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 3 other ancestors2 generations back: 8 other ancestors3 generations back: 3 other ancestors4 generations back: 10 other ancestors5 generations back: 22 other ancestors6 generations back: 8 other ancestors7 generations back: 3 other ancestors8 generations back: 1 other ancestor 1 generation forward: 1 descendant K060567 · Spectragenics Ats-1 · Spectragenics, Inc. · 2006K041086 · Palomar Starlux Pulsed Light System · Palomar Medical Products, Inc. · 2005K020839 · Quantum, Models SR, HR, DL; Vasculight, Models SR, HR, VS, VX, DL · Lumenis, Inc. · 2002K991935 · Epilight Hair Removal System, Photoderm HR System · Esc Medical Systems, Ltd. · 2000K974536 · 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. · 1992−50
  1. Root · 8 generations backK910422 Model RD-1200 Ruby Laser SystemSpectrum Medical Technologies, Inc. · 1992
  2. 7 generations backK961279 Sharplan Lasers, Inc. Ruby Laser SystemSharplan Lasers, Inc. · 1996
  3. 6 generations backK962446 Sharplan Ruby Laser SystemSharplan Lasers, Inc. · 1997
  4. 5 generations backK974536 Photoderm HR SystemEsc Medical Systems, Ltd. · 1998
  5. 4 generations backK991935 Epilight Hair Removal System, Photoderm HR SystemEsc Medical Systems, Ltd. · 2000
  6. 3 generations backK020839 Quantum, Models SR, HR, DL; Vasculight, Models SR, HR, VS, VX, DLLumenis, Inc. · 2002
  7. 2 generations backK041086 Palomar Starlux Pulsed Light SystemPalomar Medical Products, Inc. · 2005
  8. 1 generation backK060567 Spectragenics Ats-1Spectragenics, Inc. · 2006
  9. This deviceK090312 Tria Acne Treatment System, Model Ats-1 OtcTria Beauty, Inc. · 2010
  10. Descendant · cites it directly · 0 of its ownK160821 Tria SapphireTria Beauty, Inc. · 2016

Most influential descendants

Showing 1 of 1 · See all
  • K160821Tria SapphireTria Beauty, Inc. · 2016 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K910422Model RD-1200 Ruby Laser SystemSpectrum Medical Technologies, Inc.1992—
−7K961279Sharplan Lasers, Inc. Ruby Laser SystemSharplan Lasers, Inc.1996—
−6K962446Sharplan Ruby Laser SystemSharplan Lasers, Inc.1997—
−5K974536Photoderm HR SystemEsc Medical Systems, Ltd.1998—
−4K991935Epilight Hair Removal System, Photoderm HR SystemEsc Medical Systems, Ltd.2000—
−3K020839Quantum, Models SR, HR, DL; Vasculight, Models SR, HR, VS, VX, DLLumenis, Inc.2002—
−2K041086Palomar Starlux Pulsed Light SystemPalomar Medical Products, Inc.2005—
−1K060567Spectragenics Ats-1Spectragenics, Inc.2006—
0 (this device)K090312Tria Acne Treatment System, Model Ats-1 OtcTria Beauty, Inc.2010—
+1K160821Tria SapphireTria Beauty, Inc.2016—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199130
199330
199470
199560
199670
199760
199850
199930
200030
200120
200210
200340
200420
200520
200610
200710
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
FIG. 1 — Lineage of K090312, 1992–2016Source: 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? (4)

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
*K060567Spectragenics Ats-1
Summary page 1
…l, Powered Regulation Number: 21 C.F.R. § 878.481 0 Product Code: GEX Predicate Devices ATS-lI by TRIA Beauty, Inc. (formerly SpectraGenics, Inc.) (K060567) ThermaClear by Therative, Inc. (K060653) Zeno by Tyrell, Inc. (K043377) Tanda by Pharos Life Corporation (K080…
Spectragenics, Inc.2006—
*K060653Thermaclear
Summary page 1
…§ 878.481 0 Product Code: GEX Predicate Devices ATS-lI by TRIA Beauty, Inc. (formerly SpectraGenics, Inc.) (K060567) ThermaClear by Therative, Inc. (K060653) Zeno by Tyrell, Inc. (K043377) Tanda by Pharos Life Corporation (K080591)…
Dermacare, Inc.2006—
*K043377ZENO
Summary page 1
…Predicate Devices ATS-lI by TRIA Beauty, Inc. (formerly SpectraGenics, Inc.) (K060567) ThermaClear by Therative, Inc. (K060653) Zeno by Tyrell, Inc. (K043377) Tanda by Pharos Life Corporation (K080591)…
Tyrell, Inc.2005—
*K080591Tanda Skincare System, Model: Ptscs
Summary page 1
…Inc. (formerly SpectraGenics, Inc.) (K060567) ThermaClear by Therative, Inc. (K060653) Zeno by Tyrell, Inc. (K043377) Tanda by Pharos Life Corporation (K080591) 21 Intended Use I Indications f…
Pharos Life Corporation2008—

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K160821Tria SapphireTria Beauty, Inc.20160

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 18 years and passes through 7 companies; a new generation was cleared every 2.3 years on median.
  • 1 of the 66 ancestors has a recall of any class.
  • Of its descendants, K160821 (Tria Beauty, Inc., 2016) has gone furthest, with 0 descendants of its own.

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. 2010, 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 TRIA Beauty ATS-1I OTC is generally indicated to treat dermatological conditions and specifically indicated to treat mild to moderate inflammatory acne vulgaris.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K090312: Tria Acne Treatment System, Model Ats-1 Otc.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K090312

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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