# K180320: dpl IIa Panel

- Pathway: 510(k) (Traditional)
- Applicant: Led Technologies, Inc.
- Decided: Apr 3, 2018 after 57 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: 14 generations back to K943450 (1995). 108 ancestors in all.
14 later devices descend from it; 2 cite it directly.
0 of 123 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K171390: dpl II Panel, Led Technologies, Inc. (2017) Summary page 5.
- K124042: Tanda Mini Skincare System, Syneron Beauty (2013) Summary page 5.
- K121435: Silkn Blue, Home Skinovations, Ltd. (2013) Summary page 5.
- K160691: Acne Light Therapy Wand, Zuko, Inc. (2016) Summary page 5.

## Most influential descendants
- K183247: dpl Faceware (2019), 10 descendants of its own
- K230042: Q-Rejuvalight Pro Facewear (Model: P19-0023) (2023), 9 descendants of its own
- K210968: reVive Light Therapy Essentials (2021), 3 descendants of its own
- K251588: LED Light Therapy Mask (FCM902, FCM905, FCM906, FCM908, 11-001-RBMASK, FCM910) (2025), 2 descendants of its own
- K223482: reVive Light Therapy® Wrinkle and Acne LED Device (2022), 2 descendants of its own

## Indications for use
The dpl® Ila Panel is an Over-the Counter (OTC) device intended for use in treating wrinkles, and treatment of mild to moderate inflammatory acne.

Source page: https://510kreport.com/device/K180320
Methodology: https://510kreport.com/methodology