# K171390: dpl II Panel

- Pathway: 510(k) (Traditional)
- Applicant: Led Technologies, Inc.
- Decided: Aug 3, 2017 after 84 days
- Product code: OHS (Light Based Over The Counter Wrinkle Reduction)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K101190 (2010). 5 ancestors in all.
28 later devices descend from it; 6 cite it directly.
0 of 34 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141181: Nuve for Wrinkles, DPL Nuve for Wrinkles, Led Technologies, LLC (2015) Summary page 5.

## Most influential descendants
- K180320: dpl IIa Panel (2018), 14 descendants of its own
- K183247: dpl Faceware (2019), 10 descendants of its own
- K230042: Q-Rejuvalight Pro Facewear (Model: P19-0023) (2023), 9 descendants of its own
- K180445: reVive Light Therapy LED Ultrasonic Wrinkle System (2018), 5 descendants of its own
- K223147: myLEDmask (2023), 4 descendants of its own

## Indications for use
The dpl® II Panel system is an Over-the Counter (OTC) device intended for use in treating wrinkles.

Source page: https://510kreport.com/device/K171390
Methodology: https://510kreport.com/methodology