510(k) · Cleared
Cleareddpl II Panel
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Led Technologies, Inc. · OHS Light Based Over The Counter Wrinkle Reduction
Cleared on Aug 3, 2017 as substantially equivalent to K141181 (Led Technologies, LLC, 2015) after an 84-day review. Its family tree reaches back 4 generations to 2010. 28 later devices descend from it.
- Decided
- Aug 3, 2017
- Review
- 84 days
- Class
- Class II
- Product code
- OHS
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K101190 (2010). 5 ancestors in all. 28 later devices descend from it, 6 citing it directly.
- Root · 4 generations backK101190 Lightstim Anti-Wrinkle Otc Model Aal OtcLed Intellectual Properties, LLC · 2010
- 3 generations backK120775 Light for WrinklesLed Intellectual Properties, LLC · 2012
- 2 generations backK120560 Trinity Wrinkle RemoverCarol Cole Company · 2012
- 1 generation backK141181 Nuve for Wrinkles, DPL Nuve for WrinklesLed Technologies, LLC · 2015
- This deviceK171390 dpl II PanelLed Technologies, Inc. · 2017
- Descendant · cites it directly · 14 of its ownK180320 dpl IIa PanelLed Technologies, Inc. · 2018
- Descendant · 2 generations on · 10 of its ownK183247 dpl FacewareLed Technologies, Inc. · 2019
- Descendant · cites it directly · 9 of its ownK230042 Q-Rejuvalight Pro Facewear (Model: P19-0023)Light Tree Ventures Europe B.V. · 2023
- Descendant · cites it directly · 5 of its ownK180445 reVive Light Therapy LED Ultrasonic Wrinkle SystemLed Technologies, Inc. · 2018
- Descendant · cites it directly · 4 of its ownK223147 myLEDmaskMyblend · 2023
Showing 5 of 28 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 28 · See all- K180320dpl IIa PanelLed Technologies, Inc. · 2018 · cites it directly14descendants
- K183247dpl FacewareLed Technologies, Inc. · 2019 · 2 generations on10descendants
- K230042Q-Rejuvalight Pro Facewear (Model: P19-0023)Light Tree Ventures Europe B.V. · 2023 · cites it directly9descendants
- K180445reVive Light Therapy LED Ultrasonic Wrinkle SystemLed Technologies, Inc. · 2018 · cites it directly5descendants
- K223147myLEDmaskMyblend · 2023 · cites it directly4descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K101190 | Lightstim Anti-Wrinkle Otc Model Aal Otc | Led Intellectual Properties, LLC | 2010 | — |
| −3 | K120775 | Light for Wrinkles | Led Intellectual Properties, LLC | 2012 | — |
| −2 | K120560 | Trinity Wrinkle Remover | Carol Cole Company | 2012 | — |
| −1 | K141181 | Nuve for Wrinkles, DPL Nuve for Wrinkles | Led Technologies, LLC | 2015 | — |
| 0 (this device) | K171390 | dpl II Panel | Led Technologies, Inc. | 2017 | — |
| +1 | K180320 | dpl IIa Panel | Led Technologies, Inc. | 2018 | — |
| +2 | K183247 | dpl Faceware | Led Technologies, Inc. | 2019 | — |
| +1 | K230042 | Q-Rejuvalight Pro Facewear (Model: P19-0023) | Light Tree Ventures Europe B.V. | 2023 | — |
| +1 | K180445 | reVive Light Therapy LED Ultrasonic Wrinkle System | Led Technologies, Inc. | 2018 | — |
| +1 | K223147 | myLEDmask | Myblend | 2023 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2010 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 3 | 0 |
| 2019 | 1 | 0 |
| 2021 | 3 | 0 |
| 2022 | 3 | 0 |
| 2023 | 3 | 0 |
| 2025 | 9 | 0 |
| 2026 | 6 | 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? (1)
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 |
|---|---|---|---|
| * | K141181 | Nuve for Wrinkles, DPL Nuve for WrinklesSummary page 5…TC, 5. Predicate Device: This device is substantially equivalent to the following predicate, which is currently in safe and effective commerce under product code QHS: K141181 - dpl® Nuve for Wrinkles (LED Technologies, Inc.) Predicate Chart Device dpl® Il Panel dpl® Nive for Wrinkles LED Technalegies,… | 2015 |
What descends from it? (28)
See all 286 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 7 years and passes through 4 companies; a new generation was cleared every 2.3 years on median.
- None of the 5 ancestors has a recall.
- Of its descendants, K180320 (Led Technologies, Inc., 2018) has gone furthest, with 14 descendants of its own.
- 4 other devices also cite its predicate K141181.
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. 2017, 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?
The dpl® II Panel system is an Over-the Counter (OTC) device intended for use in treating wrinkles.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K171390 · printed Nov 6, 2026
Cite this page
510(k) Report. “K171390: dpl II Panel.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K171390
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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