510(k) Report

510(k) · Cleared

Cleared

Ipl Therapy System

K101901510(k) TraditionalCleared Mar 8, 2011243-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

Beijing Starlight Science & Technology Development · ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

Cleared on Mar 8, 2011 as substantially equivalent to K091664 (Shenzhen Gsd Tech Co., Ltd., 2009) and 1 other predicate after a 243-day review. Its family tree reaches back 12 generations to 1992.

Decided
Mar 8, 2011
Review
243 days
Class
Class II
Product code
ONF
Recalls
None
Predicates
2

Its longest line of descent runs back 12 generations to K910422 (1992). 87 ancestors in all, the oldest K892514 (1990). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2009: 1 other ancestor2003: 4 other ancestors2006: 2 other ancestors2005: 2 other ancestors2004: 5 other ancestors2002: 9 other ancestors2001: 4 other ancestors2000: 7 other ancestors1999: 3 other ancestors1998: 5 other ancestors1997: 6 other ancestors1996: 7 other ancestors1995: 6 other ancestors1994: 7 other ancestors1993: 3 other ancestors1991: 3 other ancestors1990: 1 other ancestorK910422 · 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. · 2003K032460 · Profile BBL System · Sciton, Inc · 2003K050047 · Cutera Optional Pulsed Light Hand Piece Family · Cutera, Inc. · 2005K051508 · Med Flash II Intense Pulsed Light System. · General Project S.R.L. · 2005K072331 · Radiancy Mistral Device · Radiancy (Israel), Ltd. · 2008K091664 · GSD Intense Pulsed Light System, Models: GP666C4, GP666C · Shenzhen Gsd Tech Co., Ltd. · 200919901995200020052010
  1. Root · 12 generations backK910422 Model RD-1200 Ruby Laser SystemSpectrum Medical Technologies, Inc. · 1992
  2. 8 generations between
  3. 3 generations backK051508 Med Flash II Intense Pulsed Light System.General Project S.R.L. · 2005
  4. 2 generations backK072331 Radiancy Mistral DeviceRadiancy (Israel), Ltd. · 2008
  5. 1 generation backK091664 GSD Intense Pulsed Light System, Models: GP666C4, GP666CShenzhen Gsd Tech Co., Ltd. · 2009
  6. This deviceK101901 Ipl Therapy SystemBeijing Starlight Science & Technology Development · 2011
Show all 12 generations
  1. Root · 12 generations backK910422 Model RD-1200 Ruby Laser SystemSpectrum Medical Technologies, Inc. · 1992
  2. 11 generations backK961279 Sharplan Lasers, Inc. Ruby Laser SystemSharplan Lasers, Inc. · 1996
  3. 10 generations backK962446 Sharplan Ruby Laser SystemSharplan Lasers, Inc. · 1997
  4. 9 generations backK974536 Photoderm HR SystemEsc Medical Systems, Ltd. · 1998
  5. 8 generations backK013366 Prolite Pulsed Light System for the Removal of Unwanted HairMedical Bio Care Sweden AB · 2002
  6. 7 generations backK022568 Prolite/Plasmalite MPX Pulsed Light System for Treatment of Unwanted…Medical Bio Care Sweden AB · 2002
  7. 6 generations backK023954 Altus Medical Coolglide Laser Systems and AccessoriesAltus Medical, Inc. · 2003
  8. 5 generations backK032460 Profile BBL SystemSciton, Inc · 2003
  9. 4 generations backK050047 Cutera Optional Pulsed Light Hand Piece FamilyCutera, Inc. · 2005
  10. 3 generations backK051508 Med Flash II Intense Pulsed Light System.General Project S.R.L. · 2005
  11. 2 generations backK072331 Radiancy Mistral DeviceRadiancy (Israel), Ltd. · 2008
  12. 1 generation backK091664 GSD Intense Pulsed Light System, Models: GP666C4, GP666CShenzhen Gsd Tech Co., Ltd. · 2009
  13. This deviceK101901 Ipl Therapy SystemBeijing Starlight Science & Technology Development · 2011
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−12K910422Model RD-1200 Ruby Laser SystemSpectrum Medical Technologies, Inc.1992—
−11K961279Sharplan Lasers, Inc. Ruby Laser SystemSharplan Lasers, Inc.1996—
−10K962446Sharplan Ruby Laser SystemSharplan Lasers, Inc.1997—
−9K974536Photoderm HR SystemEsc Medical Systems, Ltd.1998—
−8K013366Prolite Pulsed Light System for the Removal of Unwanted HairMedical Bio Care Sweden AB2002—
−7K022568Prolite/Plasmalite MPX Pulsed Light System for Treatment of Unwanted HairMedical Bio Care Sweden AB2002—
−6K023954Altus Medical Coolglide Laser Systems and AccessoriesAltus Medical, Inc.2003—
−5K032460Profile BBL SystemSciton, Inc2003—
−4K050047Cutera Optional Pulsed Light Hand Piece FamilyCutera, Inc.2005—
−3K051508Med Flash II Intense Pulsed Light System.General Project S.R.L.2005—
−2K072331Radiancy Mistral DeviceRadiancy (Israel), Ltd.2008—
−1K091664GSD Intense Pulsed Light System, Models: GP666C4, GP666CShenzhen Gsd Tech Co., Ltd.2009—
0 (this device)K101901Ipl Therapy SystemBeijing Starlight Science & Technology Development2011—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199130
199330
199470
199560
199670
199760
199850
199930
200070
200140
200290
200340
200450
200520
200620
200910
FIG. 1 — Lineage of K101901, 1992–2011Source: 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 ONF? 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 ONF device

  1. #1 K233473 Deka Lotusscore 18.1 · 27 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K091664GSD Intense Pulsed Light System, Models: GP666C4, GP666C
Summary page 1
…21 CFR 878.4810 Device Class: Class 11 Submission Purpose: New Device Predicate Device: GSD INTENSE PULSED LIGHT SYSTEM (K091664) Angelite Family of Intense Pulsed Light System (K08391I5) Device Description Th…
Shenzhen Gsd Tech Co., Ltd.2009—
*K083915Angelite Family of Intense Pulsed Light Systems, Models Angelite-DDC and Angelite-SDCAdvanced Technology Laser Co., Ltd.2009—

Also cleared against K091664: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

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 11 companies; a new generation was cleared every 1.3 years on median.
  • 1 of the 87 ancestors has a recall of any class.
  • 1 other device also cites its predicate K091664.

How does its category compare?

All ONF devices

ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · ONF

4in 2025

2008: 12009: 52010: 42011: 52012: 32013: 102014: 72015: 32016: 52018: 22019: 22020: 42021: 42022: 42023: 52024: 52025: 42026 (partial year): 1
2007high 10 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ONF

192in 2025

2009: 160 days median2010: 137 days median2011: 166 days median2012: 134 days median2013: 113 days median2014: 118 days median2015: 111 days median2016: 87 days median2020: 104 days median2021: 101 days median2022: 165 days median2023: 86 days median2024: 168 days median2025: 192 days median
2007high 192 (2025) · low 86 (2023)2026

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

Recalls per year · ONF

No recall names ONF since 2007.

Adverse event reports per year · ONF

5in 2025

2014: 22015: 42016: 62017: 12018: 12019: 22020: 12021: 22022: 22023: 22024: 32025: 5
2007high 6 (2016) · low 0 (2007)2025

MAUDE reports naming product code ONF, 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
20070—00
20081—00
2009516000
2010413700
2011516600
2012313400
20131011300
2014711802
2015311104
201658706
20170—01
20182—01
20192—02
2020410401
2021410102
2022416502
202358602
2024516803
2025419205
20261—0—

What is it indicated for?

The IPL Therapy Systems (inclusive of the handpieces used to deliver pulsed-light energy) is indicated for use in surgical, aesthetic and cosmetic applications in the hair removal.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K101901: Ipl Therapy System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K101901

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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