510(k) Report

510(k) · Cleared

Cleared

reVive Light Therapy LED Cleansing System

K221430510(k) SpecialCleared Jul 27, 202271-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

Led Technologies, Inc. · OHS Light Based Over The Counter Wrinkle Reduction

Cleared on Jul 27, 2022 as substantially equivalent to K180445 (Led Technologies, Inc., 2018) and 1 other predicate after a 71-day review. Its family tree reaches back 15 generations to 1995.

Decided
Jul 27, 2022
Review
71 days
Class
Class II
Product code
OHS
Recalls
None
Predicates
2

Its longest line of descent runs back 15 generations to K943450 (1995). 118 ancestors in all, the oldest K800617 (1980). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2018: 1 other ancestor2017: 1 other ancestor2016: 1 other ancestor2015: 1 other ancestor2013: 2 other ancestors2012: 2 other ancestors2010: 3 other ancestors2009: 1 other ancestor2008: 1 other ancestor2006: 1 other ancestor2005: 3 other ancestors2003: 4 other ancestors2007: 2 other ancestors2002: 4 other ancestors2001: 1 other ancestor2000: 6 other ancestors1999: 4 other ancestors1998: 11 other ancestors1996: 12 other ancestors1995: 9 other ancestors1997: 13 other ancestors1994: 8 other ancestors1993: 3 other ancestors1991: 3 other ancestors1990: 1 other ancestor1980: 1 other ancestor1992: 3 other ancestors1985: 1 other ancestorK943450 · Arthrocare Arthroscopic Electrosurgery System Model 970 · Arthrocare Corp. · 1995×2: 2 generations cleared close together, K961069 (1996), K962445 (1996) ×2: 2 generations cleared close together, K964849 (1997), K971532 (1997) K974521 · Vnus Closure System · Vnus Medical Technologies, Inc. · 1998K982816 · Vnus Closure System · Vnus Medical Technologies, Inc. · 1999K022266 · Aurora SR · Syneron Medical, Ltd. · 2002K030426 · Omnilux Red · Photo Therapeutics Limited · 2003K050216 · Omnilux Revive and Omnilux Plus · Photo Therapeutics Limited · 2005K072459 · Omnilux New-U · Photo Therapeutics, Inc. · 2008K110301 · Silk'n FX · Home Skinovations, Ltd. · 2011K152332 · Perfectio LED infrared device · Omm Imports Inc Dba Zero Gravity · 2016K162489 · RED Light Device · Zhongshan Bisen Plastic Electronic Products Co., Ltd. · 2017K180445 · reVive Light Therapy LED Ultrasonic Wrinkle System · Led Technologies, Inc. · 201819801990200020102020
Other ancestors, by generation 1 generation back: 1 other ancestor2 generations back: 3 other ancestors3 generations back: 6 other ancestors4 generations back: 6 other ancestors5 generations back: 8 other ancestors6 generations back: 20 other ancestors7 generations back: 25 other ancestors8 generations back: 18 other ancestors9 generations back: 14 other ancestors10 generations back: 2 other ancestors K180445 · reVive Light Therapy LED Ultrasonic Wrinkle System · Led Technologies, Inc. · 2018K162489 · RED Light Device · Zhongshan Bisen Plastic Electronic Products Co., Ltd. · 2017K152332 · Perfectio LED infrared device · Omm Imports Inc Dba Zero Gravity · 2016K110301 · Silk'n FX · Home Skinovations, Ltd. · 2011K072459 · Omnilux New-U · Photo Therapeutics, Inc. · 2008K050216 · Omnilux Revive and Omnilux Plus · Photo Therapeutics Limited · 2005K030426 · Omnilux Red · Photo Therapeutics Limited · 2003K022266 · Aurora SR · Syneron Medical, Ltd. · 2002K982816 · Vnus Closure System · Vnus Medical Technologies, Inc. · 1999K974521 · Vnus Closure System · Vnus Medical Technologies, Inc. · 1998K971532 · Arthrocare Electrosurgery System · Arthrocare Corp. · 1997K964849 · Arthrocare Dermatologic Electrosurgery System · Arthrocare Corp. · 1997K962445 · Arthrocare Dental Electrosurgery System · Arthrocare Corp. · 1996K961069 · Arthrocare Urologic Multi-Electrode Electrosurgery System · Arthrocare Corp. · 1996K943450 · Arthrocare Arthroscopic Electrosurgery System Model 970 · Arthrocare Corp. · 1995−15−10−50
  1. Root · 15 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 11 generations between
  3. 3 generations backK152332 Perfectio LED infrared deviceOmm Imports Inc Dba Zero Gravity · 2016
  4. 2 generations backK162489 RED Light DeviceZhongshan Bisen Plastic Electronic Products Co., Ltd. · 2017
  5. 1 generation backK180445 reVive Light Therapy LED Ultrasonic Wrinkle SystemLed Technologies, Inc. · 2018
  6. This deviceK221430 reVive Light Therapy LED Cleansing SystemLed Technologies, Inc. · 2022
Show all 15 generations
  1. Root · 15 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
  2. 14 generations backK961069 Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp. · 1996
  3. 13 generations backK962445 Arthrocare Dental Electrosurgery SystemArthrocare Corp. · 1996
  4. 12 generations backK964849 Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp. · 1997
  5. 11 generations backK971532 Arthrocare Electrosurgery SystemArthrocare Corp. · 1997
  6. 10 generations backK974521 Vnus Closure SystemVnus Medical Technologies, Inc. · 1998
  7. 9 generations backK982816 Vnus Closure SystemVnus Medical Technologies, Inc. · 1999
  8. 8 generations backK022266 Aurora SRSyneron Medical, Ltd. · 2002
  9. 7 generations backK030426 Omnilux RedPhoto Therapeutics Limited · 2003
  10. 6 generations backK050216 Omnilux Revive and Omnilux PlusPhoto Therapeutics Limited · 2005
  11. 5 generations backK072459 Omnilux New-UPhoto Therapeutics, Inc. · 2008
  12. 4 generations backK110301 Silk'n FXHome Skinovations, Ltd. · 2011
  13. 3 generations backK152332 Perfectio LED infrared deviceOmm Imports Inc Dba Zero Gravity · 2016
  14. 2 generations backK162489 RED Light DeviceZhongshan Bisen Plastic Electronic Products Co., Ltd. · 2017
  15. 1 generation backK180445 reVive Light Therapy LED Ultrasonic Wrinkle SystemLed Technologies, Inc. · 2018
  16. This deviceK221430 reVive Light Therapy LED Cleansing SystemLed Technologies, Inc. · 2022
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−15K943450Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp.1995—
−14K961069Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp.1996—
−13K962445Arthrocare Dental Electrosurgery SystemArthrocare Corp.1996—
−12K964849Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp.1997—
−11K971532Arthrocare Electrosurgery SystemArthrocare Corp.1997—
−10K974521Vnus Closure SystemVnus Medical Technologies, Inc.1998—
−9K982816Vnus Closure SystemVnus Medical Technologies, Inc.1999—
−8K022266Aurora SRSyneron Medical, Ltd.2002—
−7K030426Omnilux RedPhoto Therapeutics Limited2003—
−6K050216Omnilux Revive and Omnilux PlusPhoto Therapeutics Limited2005—
−5K072459Omnilux New-UPhoto Therapeutics, Inc.2008—
−4K110301Silk'n FXHome Skinovations, Ltd.2011—
−3K152332Perfectio LED infrared deviceOmm Imports Inc Dba Zero Gravity2016—
−2K162489RED Light DeviceZhongshan Bisen Plastic Electronic Products Co., Ltd.2017—
−1K180445reVive Light Therapy LED Ultrasonic Wrinkle SystemLed Technologies, Inc.2018—
0 (this device)K221430reVive Light Therapy LED Cleansing SystemLed Technologies, Inc.2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
198510
199010
199130
199230
199330
199480
199590
1996120
1997130
1998110
199940
200060
200110
200240
200340
200530
200610
200720
200810
200910
201030
201220
201320
201510
201610
201710
201810
FIG. 1 — Lineage of K221430, 1995–2022Source: 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
*K180445reVive Light Therapy LED Ultrasonic Wrinkle System
Summary page 5
…cate Device This device is substantially equivalent to the following predicates, which are currently in safe and effective commerce under product codes OHS/OLP: K180445 – The reVive Light Therapy® LED Cleansing System (LED Technologies, Inc.) K180447 – The reVive Light Therapy® LED Cleansing Sy…
Led Technologies, Inc.2018—
*K180447reVive Light Therapy LED Cleansing System
Summary page 5
…hich are currently in safe and effective commerce under product codes OHS/OLP: K180445 – The reVive Light Therapy® LED Cleansing System (LED Technologies, Inc.) K180447 – The reVive Light Therapy® LED Cleansing System (LED Technologies, Inc.) Comparison Chart New Device…
Led Technologies, Inc.2018—

Also cleared against K180445: 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 27 years and passes through 9 companies; a new generation was cleared every 1.2 years on median.
  • 3 of the 118 ancestors have a recall of any class.
  • 1 other device also cites its predicate K180445.

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. 2022, 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 reVive Light Therapy LED Cleansing System is intended for treatment of wrinkles and mild to moderate inflammatory acne.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K221430: reVive Light Therapy LED Cleansing System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K221430

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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