510(k) · Cleared
ClearedPlatinumgmt Ipl System Cloud
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Global Medical Technology S.L. · ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
Cleared on Dec 19, 2014 as substantially equivalent to K131859 (Beijing Honkon Technologies Co., Ltd., 2013) and 1 other predicate after a 276-day review. Its family tree reaches back 13 generations to 1992. 2 later devices descend from it.
- Decided
- Dec 19, 2014
- Review
- 276 days
- Class
- Class II
- Product code
- ONF
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 13 generations to K910422 (1992). 92 ancestors in all, the oldest K885026 (1989). 2 later devices descend from it, 1 citing it directly.
- Root · 13 generations backK910422 Model RD-1200 Ruby Laser SystemSpectrum Medical Technologies, Inc. · 1992
- 9 generations between
- 3 generations backK093627 Ipulselight Ipl System, Models HS 300C and HS 650Shanghai Apolo Medical Technologies Co., Ltd. · 2011
- 2 generations backK122995 Intense Pulsed Light (Ipl) SystemsBeijing Kes Biology Technology Co., Ltd. · 2013
- 1 generation backK131859 Multifunctional SeriesBeijing Honkon Technologies Co., Ltd. · 2013
- This deviceK140668 Platinumgmt Ipl System CloudGlobal Medical Technology S.L. · 2014
- Descendant · cites it directly · 1 of its ownK153717 Venus Versa SystemVenus Concept, Ltd. · 2016
- Descendant · 2 generations on · 0 of its ownK232192 Venus Versa PRO SystemVenus Concept, Inc. · 2023
Show all 13 generations
- Root · 13 generations backK910422 Model RD-1200 Ruby Laser SystemSpectrum Medical Technologies, Inc. · 1992
- 12 generations backK961279 Sharplan Lasers, Inc. Ruby Laser SystemSharplan Lasers, Inc. · 1996
- 11 generations backK962446 Sharplan Ruby Laser SystemSharplan Lasers, Inc. · 1997
- 10 generations backK974536 Photoderm HR SystemEsc Medical Systems, Ltd. · 1998
- 9 generations backK013366 Prolite Pulsed Light System for the Removal of Unwanted HairMedical Bio Care Sweden AB · 2002
- 8 generations backK022568 Prolite/Plasmalite MPX Pulsed Light System for Treatment of Unwanted…Medical Bio Care Sweden AB · 2002
- 7 generations backK023954 Altus Medical Coolglide Laser Systems and AccessoriesAltus Medical, Inc. · 2003
- 6 generations backK033946 Lovely SystemMsq (M2), Ltd. · 2004
- 5 generations backK053324 Chromolite SystemChromogenex Plc · 2006
- 4 generations backK082484 Accelawave SystemGenesis Biosystems, Inc. · 2008
- 3 generations backK093627 Ipulselight Ipl System, Models HS 300C and HS 650Shanghai Apolo Medical Technologies Co., Ltd. · 2011
- 2 generations backK122995 Intense Pulsed Light (Ipl) SystemsBeijing Kes Biology Technology Co., Ltd. · 2013
- 1 generation backK131859 Multifunctional SeriesBeijing Honkon Technologies Co., Ltd. · 2013
- This deviceK140668 Platinumgmt Ipl System CloudGlobal Medical Technology S.L. · 2014
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −13 | K910422 | Model RD-1200 Ruby Laser System | Spectrum Medical Technologies, Inc. | 1992 | — |
| −12 | K961279 | Sharplan Lasers, Inc. Ruby Laser System | Sharplan Lasers, Inc. | 1996 | — |
| −11 | K962446 | Sharplan Ruby Laser System | Sharplan Lasers, Inc. | 1997 | — |
| −10 | K974536 | Photoderm HR System | Esc Medical Systems, Ltd. | 1998 | — |
| −9 | K013366 | Prolite Pulsed Light System for the Removal of Unwanted Hair | Medical Bio Care Sweden AB | 2002 | — |
| −8 | K022568 | Prolite/Plasmalite MPX Pulsed Light System for Treatment of Unwanted Hair | Medical Bio Care Sweden AB | 2002 | — |
| −7 | K023954 | Altus Medical Coolglide Laser Systems and Accessories | Altus Medical, Inc. | 2003 | — |
| −6 | K033946 | Lovely System | Msq (M2), Ltd. | 2004 | — |
| −5 | K053324 | Chromolite System | Chromogenex Plc | 2006 | — |
| −4 | K082484 | Accelawave System | Genesis Biosystems, Inc. | 2008 | — |
| −3 | K093627 | Ipulselight Ipl System, Models HS 300C and HS 650 | Shanghai Apolo Medical Technologies Co., Ltd. | 2011 | — |
| −2 | K122995 | Intense Pulsed Light (Ipl) Systems | Beijing Kes Biology Technology Co., Ltd. | 2013 | — |
| −1 | K131859 | Multifunctional Series | Beijing Honkon Technologies Co., Ltd. | 2013 | — |
| 0 (this device) | K140668 | Platinumgmt Ipl System Cloud | Global Medical Technology S.L. | 2014 | — |
| +1 | K153717 | Venus Versa System | Venus Concept, Ltd. | 2016 | — |
| +2 | K232192 | Venus Versa PRO System | Venus Concept, Inc. | 2023 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1989 | 1 | 0 |
| 1990 | 1 | 0 |
| 1991 | 3 | 0 |
| 1993 | 6 | 0 |
| 1994 | 7 | 0 |
| 1995 | 7 | 0 |
| 1996 | 7 | 0 |
| 1997 | 8 | 0 |
| 1998 | 6 | 0 |
| 1999 | 4 | 0 |
| 2000 | 7 | 0 |
| 2001 | 7 | 0 |
| 2002 | 9 | 0 |
| 2003 | 6 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2016 | 1 | 0 |
| 2023 | 1 | 0 |
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 K233473 Deka Lotusscore 18.1 · 27 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K131859 | Multifunctional SeriesSummary page 5…-------- Pigmented Lesions 560-1200 560-1200 560-1200 560-1200 ------------ 5. Predicate Device Identification 510(k) Number: K131859 Product Name: Multifunctional Series Manufacturer: Beijing Honkon Technologies Co., Ltd. 510(k) Number: K122995 Product Name: Int… | 2013 |
| * | K122995 | Intense Pulsed Light (Ipl) SystemsSummary page 5…---- 5. Predicate Device Identification 510(k) Number: K131859 Product Name: Multifunctional Series Manufacturer: Beijing Honkon Technologies Co., Ltd. 510(k) Number: K122995 Product Name: Intense Pulse Light (IPL) Systems/ MED-210/230 Manufacturer: Beijing Kes Biology Technology Co., Ltd.… | 2013 |
What descends from it? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K153717 | Venus Versa System | 2016 | 1 |
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 22 years and passes through 12 companies; a new generation was cleared every 1.2 years on median.
- 2 of the 92 ancestors have a recall of any class.
- Of its descendants, K153717 (Venus Concept, Ltd., 2016) has gone furthest, with 1 descendant of its own.
How does its category compare?
All ONF devicesONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.
FDA decisions per year · ONF
4in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · ONF
192in 2025
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
MAUDE reports naming product code ONF, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 1 | — | 0 | 0 |
| 2009 | 5 | 160 | 0 | 0 |
| 2010 | 4 | 137 | 0 | 0 |
| 2011 | 5 | 166 | 0 | 0 |
| 2012 | 3 | 134 | 0 | 0 |
| 2013 | 10 | 113 | 0 | 0 |
| 2014 | 7 | 118 | 0 | 2 |
| 2015 | 3 | 111 | 0 | 4 |
| 2016 | 5 | 87 | 0 | 6 |
| 2017 | 0 | — | 0 | 1 |
| 2018 | 2 | — | 0 | 1 |
| 2019 | 2 | — | 0 | 2 |
| 2020 | 4 | 104 | 0 | 1 |
| 2021 | 4 | 101 | 0 | 2 |
| 2022 | 4 | 165 | 0 | 2 |
| 2023 | 5 | 86 | 0 | 2 |
| 2024 | 5 | 168 | 0 | 3 |
| 2025 | 4 | 192 | 0 | 5 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The PlatinumGMT™ IPL System Cloud device (inclusive of the
hand piece used to deliver pulsed-light energy) is indicated for use in surgical,
aesthetic and cosmetic applications in permanent hair reduction, moderate
inflammatory acne vulgaris, benign cutaneous pigmented and vascular lesions.
Permanent hair reduction is defined as the long-term stable reduction in the number of hairs
regrowing when measured at 6, 9, and 12 months after the completion of a treatment regimen.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K140668 · printed Nov 6, 2026
Cite this page
510(k) Report. “K140668: Platinumgmt Ipl System Cloud.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K140668
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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