510(k) · Cleared
ClearedJmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Shenzhen Ulike Smart Electronics Co., Ltd. · OHS Light Based Over The Counter Wrinkle Reduction
Cleared on Oct 1, 2025 as substantially equivalent to K223919 (Bemer Int AG, 2023) and 2 other predicates after a 110-day review. Its family tree reaches back 18 generations to 1995.
- Decided
- Oct 1, 2025
- Review
- 110 days
- Class
- Class II
- Product code
- OHS
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 18 generations to K943450 (1995). 286 ancestors in all, the oldest K800617 (1980). No later device cites it as a predicate yet.
- Root · 18 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
- 14 generations between
- 3 generations backK190443 MMSphereGalactic Beauty, LLC · 2019
- 2 generations backK202390 Aduro Light Beauty MaskShenzhen Kaiyan Medical CO, Ltd. · 2021
- 1 generation backK223919 B.Light Clear Evo and B.Light Restore EvoBemer Int AG · 2023
- This deviceK251825 Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)Shenzhen Ulike Smart Electronics Co., Ltd. · 2025
Show all 18 generations
- Root · 18 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
- 17 generations backK961069 Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp. · 1996
- 16 generations backK962445 Arthrocare Dental Electrosurgery SystemArthrocare Corp. · 1996
- 15 generations backK964849 Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp. · 1997
- 14 generations backK971532 Arthrocare Electrosurgery SystemArthrocare Corp. · 1997
- 13 generations backK974521 Vnus Closure SystemVnus Medical Technologies, Inc. · 1998
- 12 generations backK982816 Vnus Closure SystemVnus Medical Technologies, Inc. · 1999
- 11 generations backK022266 Aurora SRSyneron Medical, Ltd. · 2002
- 10 generations backK030426 Omnilux RedPhoto Therapeutics Limited · 2003
- 9 generations backK081307 Omnilux Clear-UPhoto Therapeutics, Inc. · 2009
- 8 generations backK123999 Illumask Acne Light Therapy MaskLa Lumiere, LLC · 2013
- 7 generations backK140471 Pro X Otc 5La Lumiere, LLC · 2015
- 6 generations backK163329 Pulsaderm Wrinkle Mask 28, Pulsaderm Wrinkle Mask 72Pulsaderm, LLC · 2017
- 5 generations backK170984 LG Beauty Led MaskLg Electronics · 2017
- 4 generations backK180856 Neutrogena Light Therapy Aging Mask+Johnson & Johnson Consumer, Inc. · 2018
- 3 generations backK190443 MMSphereGalactic Beauty, LLC · 2019
- 2 generations backK202390 Aduro Light Beauty MaskShenzhen Kaiyan Medical CO, Ltd. · 2021
- 1 generation backK223919 B.Light Clear Evo and B.Light Restore EvoBemer Int AG · 2023
- This deviceK251825 Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)Shenzhen Ulike Smart Electronics Co., Ltd. · 2025
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −18 | K943450 | Arthrocare Arthroscopic Electrosurgery System Model 970 | Arthrocare Corp. | 1995 | — |
| −17 | K961069 | Arthrocare Urologic Multi-Electrode Electrosurgery System | Arthrocare Corp. | 1996 | — |
| −16 | K962445 | Arthrocare Dental Electrosurgery System | Arthrocare Corp. | 1996 | — |
| −15 | K964849 | Arthrocare Dermatologic Electrosurgery System | Arthrocare Corp. | 1997 | — |
| −14 | K971532 | Arthrocare Electrosurgery System | Arthrocare Corp. | 1997 | — |
| −13 | K974521 | Vnus Closure System | Vnus Medical Technologies, Inc. | 1998 | — |
| −12 | K982816 | Vnus Closure System | Vnus Medical Technologies, Inc. | 1999 | — |
| −11 | K022266 | Aurora SR | Syneron Medical, Ltd. | 2002 | — |
| −10 | K030426 | Omnilux Red | Photo Therapeutics Limited | 2003 | — |
| −9 | K081307 | Omnilux Clear-U | Photo Therapeutics, Inc. | 2009 | — |
| −8 | K123999 | Illumask Acne Light Therapy Mask | La Lumiere, LLC | 2013 | — |
| −7 | K140471 | Pro X Otc 5 | La Lumiere, LLC | 2015 | — |
| −6 | K163329 | Pulsaderm Wrinkle Mask 28, Pulsaderm Wrinkle Mask 72 | Pulsaderm, LLC | 2017 | — |
| −5 | K170984 | LG Beauty Led Mask | Lg Electronics | 2017 | — |
| −4 | K180856 | Neutrogena Light Therapy Aging Mask+ | Johnson & Johnson Consumer, Inc. | 2018 | — |
| −3 | K190443 | MMSphere | Galactic Beauty, LLC | 2019 | — |
| −2 | K202390 | Aduro Light Beauty Mask | Shenzhen Kaiyan Medical CO, Ltd. | 2021 | — |
| −1 | K223919 | B.Light Clear Evo and B.Light Restore Evo | Bemer Int AG | 2023 | — |
| 0 (this device) | K251825 | Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) | Shenzhen Ulike Smart Electronics Co., Ltd. | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1980 | 1 | 0 |
| 1982 | 1 | 0 |
| 1984 | 1 | 0 |
| 1985 | 1 | 0 |
| 1988 | 1 | 0 |
| 1989 | 2 | 0 |
| 1990 | 1 | 0 |
| 1991 | 4 | 0 |
| 1992 | 3 | 0 |
| 1993 | 8 | 0 |
| 1994 | 11 | 0 |
| 1995 | 13 | 0 |
| 1996 | 17 | 0 |
| 1997 | 20 | 0 |
| 1998 | 15 | 0 |
| 1999 | 7 | 0 |
| 2000 | 22 | 0 |
| 2001 | 23 | 0 |
| 2002 | 29 | 0 |
| 2003 | 20 | 0 |
| 2004 | 13 | 0 |
| 2005 | 12 | 0 |
| 2006 | 3 | 0 |
| 2007 | 4 | 0 |
| 2008 | 1 | 0 |
| 2009 | 2 | 0 |
| 2010 | 2 | 0 |
| 2011 | 1 | 0 |
| 2012 | 2 | 0 |
| 2013 | 4 | 0 |
| 2014 | 4 | 0 |
| 2015 | 1 | 0 |
| 2016 | 2 | 0 |
| 2017 | 2 | 0 |
| 2018 | 4 | 0 |
| 2019 | 3 | 0 |
| 2020 | 2 | 0 |
| 2021 | 2 | 0 |
| 2022 | 2 | 0 |
| 2023 | 1 | 0 |
| 2024 | 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 OHS? 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 OHS device
- #1 K223544 LED light therapy mask (FM-01, FM-02, FM-03)score 48.4 · 16 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K223919 | B.Light Clear Evo and B.Light Restore EvoSummary page 5…Predicate Predicate Predicate Devices Device 2 Device 3 510(k) number K223919 K210948 K240089 Trade Name BEMER Light BEMER Light… | 2023 |
| * | K210948 | Omnilux CLEARSummary page 5…cate Predicate Devices Device 2 Device 3 510(k) number K223919 K210948 K240089 Trade Name BEMER Light BEMER Light Omnilux Face Patches… | 2021 |
| * | K240089 | Face Patches (MT-12MA, MT-12MC)Summary page 5…ices Device 2 Device 3 510(k) number K223919 K210948 K240089 Trade Name BEMER Light BEMER Light Omnilux Face Patches Therapy… | 2024 |
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 30 years and passes through 13 companies; a new generation was cleared every 1.2 years on median.
- 12 of the 286 ancestors have a recall of any class.
- 1 other device also cites its predicate K223919.
How does its category compare?
All OHS devicesOHS Light Based Over The Counter Wrinkle Reduction: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.
FDA decisions per year · OHS
42in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · OHS
89in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · OHS
1in 2008
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · OHS
34in 2025
MAUDE reports naming product code OHS, 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 | 2 | — | 1 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 3 | 176 | 0 | 0 |
| 2011 | 2 | — | 0 | 1 |
| 2012 | 4 | 310 | 0 | 1 |
| 2013 | 2 | — | 0 | 0 |
| 2014 | 5 | 168 | 0 | 1 |
| 2015 | 4 | 241 | 0 | 0 |
| 2016 | 3 | 191 | 0 | 0 |
| 2017 | 8 | 133 | 0 | 1 |
| 2018 | 7 | 84 | 0 | 1 |
| 2019 | 4 | 99 | 0 | 1 |
| 2020 | 2 | — | 0 | 2 |
| 2021 | 7 | 162 | 0 | 2 |
| 2022 | 16 | 129 | 0 | 2 |
| 2023 | 12 | 101 | 0 | 4 |
| 2024 | 16 | 87 | 0 | 5 |
| 2025 | 42 | 89 | 0 | 34 |
| 2026 | 26 | 88 | 0 | — |
What is it indicated for?
Jmoon FlexGlow Light Therapy Device is an over the counter device that is intended:
- the Red light and Infrared light is indicated for use in the treatment of full face wrinkles,
- the Blue light and Red light indicated for the treatment of mild to moderate inflammatory acne.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K251825 · printed Nov 6, 2026
Cite this page
510(k) Report. “K251825: Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K251825
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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