510(k) Report

510(k) · Cleared

Cleared

LED Light Therapy Masks (LumiLips FAC07NA)

K260202510(k) TraditionalCleared Mar 23, 202659-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

Guangdong Newdermo Biotech Co., Ltd. · OHS Light Based Over The Counter Wrinkle Reduction

Cleared on Mar 23, 2026 as substantially equivalent to K172662 (Led Technologies, Inc., 2018) and 1 other predicate after a 59-day review. Its family tree reaches back 7 generations to 2010.

Decided
Mar 23, 2026
Review
59 days
Class
Class II
Product code
OHS
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K101190 (2010). 9 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 7 generations backK101190 Lightstim Anti-Wrinkle Otc Model Aal OtcLed Intellectual Properties, LLC · 2010
  2. 6 generations backK120775 Light for WrinklesLed Intellectual Properties, LLC · 2012
  3. 5 generations backK120560 Trinity Wrinkle RemoverCarol Cole Company · 2012
  4. 4 generations backK141181 Nuve for Wrinkles, DPL Nuve for WrinklesLed Technologies, LLC · 2015
  5. 3 generations backK171390 dpl II PanelLed Technologies, Inc. · 2017
  6. 2 generations backK172662 reVive PerioralLed Technologies, Inc. · 2018
  7. 1 generation backK213024 Oren LED Perioral Light Therapy SystemShenzhen Kaiyan Medical CO, Ltd. · 2021
  8. This deviceK260202 LED Light Therapy Masks (LumiLips FAC07NA)Guangdong Newdermo Biotech Co., Ltd. · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K101190Lightstim Anti-Wrinkle Otc Model Aal OtcLed Intellectual Properties, LLC2010—
−6K120775Light for WrinklesLed Intellectual Properties, LLC2012—
−5K120560Trinity Wrinkle RemoverCarol Cole Company2012—
−4K141181Nuve for Wrinkles, DPL Nuve for WrinklesLed Technologies, LLC2015—
−3K171390dpl II PanelLed Technologies, Inc.2017—
−2K172662reVive PerioralLed Technologies, Inc.2018—
−1K213024Oren LED Perioral Light Therapy SystemShenzhen Kaiyan Medical CO, Ltd.2021—
0 (this device)K260202LED Light Therapy Masks (LumiLips FAC07NA)Guangdong Newdermo Biotech Co., Ltd.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201010
201710
FIG. 1 — Lineage of K260202, 2010–2026Source: 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 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. #1 K223544 LED light therapy mask (FM-01, FM-02, FM-03)score 48.4 · 16 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
*K172662reVive Perioral
Summary page 5
…te Device(s): 1) Predicate device1 Sponsor: LED Technologies, Inc Device name: reVive Perioral 510(k) Number: K172662 Guangdong Newdermo Biotech Co.,Ltd 1/9 Traditional 510…
Led Technologies, Inc.2018—
*K213024Oren LED Perioral Light Therapy System
Summary page 6
…Sponsor: Shenzhen Kaiyan Medical Co Ltd. Device name: Oren LED Perioral Light Therapy System 510(k) Number: K213024 Regulation Number 21 CFR 878.4810 Light Based Over The Counter Wrinkle Reduction C…
Shenzhen Kaiyan Medical CO, Ltd.2021—

Also cleared against K172662: 3 other devices →

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 16 years and passes through 6 companies; a new generation was cleared every 2.3 years on median.
  • None of the 9 ancestors has a recall.
  • 3 other devices also cite its predicate K172662.

How does its category compare?

All OHS devices

OHS Light Based Over The Counter Wrinkle Reduction: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · OHS

42in 2025

2008: 22010: 32011: 22012: 42013: 22014: 52015: 42016: 32017: 82018: 72019: 42020: 22021: 72022: 162023: 122024: 162025: 422026 (partial year): 26
2007high 42 (2025) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OHS

89in 2025

2010: 176 days median2012: 310 days median2014: 168 days median2015: 241 days median2016: 191 days median2017: 133 days median2018: 84 days median2019: 99 days median2021: 162 days median2022: 129 days median2023: 101 days median2024: 87 days median2025: 89 days median2026 (partial year): 88 days median
2007high 310 (2012) · low 84 (2018)2026

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

Recalls per year · OHS

1in 2008

2008: 1
2007high 1 (2008) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · OHS

34in 2025

2011: 12012: 12014: 12017: 12018: 12019: 12020: 22021: 22022: 22023: 42024: 52025: 34
2007high 34 (2025) · low 0 (2007)2025

MAUDE reports naming product code OHS, 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
20082—10
20090—00
2010317600
20112—01
2012431001
20132—00
2014516801
2015424100
2016319100
2017813301
201878401
201949901
20202—02
2021716202
20221612902
20231210104
2024168705
20254289034
202626880—

What is it indicated for?

The LED Light Therapy Mask is an Over-the-Counter (OTC) device intended for treatment of fine lines and wrinkles, and increase in circulation within the perioral region.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K260202: LED Light Therapy Masks (LumiLips FAC07NA).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K260202

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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