# K183247: dpl Faceware

- Pathway: 510(k) (Traditional)
- Applicant: Led Technologies, Inc.
- Decided: Mar 14, 2019 after 113 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: 15 generations back to K943450 (1995). 112 ancestors in all.
10 later devices descend from it; 1 cites 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)
- K180320: dpl IIa Panel, Led Technologies, Inc. (2018) Summary page 5.
- K180447: reVive Light Therapy LED Cleansing System, Led Technologies, Inc. (2018) Summary page 5.
- K171386: dpl SpectraLite, Led Technologies, Inc. (2017) Summary page 5.

## Most influential descendants
- K230042: Q-Rejuvalight Pro Facewear (Model: P19-0023) (2023), 9 descendants of its own
- K251588: LED Light Therapy Mask (FCM902, FCM905, FCM906, FCM908, 11-001-RBMASK, FCM910) (2025), 2 descendants of its own
- K261370: LED Light Therapy Masks (LED Face Mask Pulse (FAC06NA)) (2026), 0 descendants of its own
- K261496: LED Light Therapy Masks (PE748, PE749, PE756) (2026), 0 descendants of its own
- K260715: CurrentBody Skin LED Multi Light Therapy Mask (MK-110D) (2026), 0 descendants of its own

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

Source page: https://510kreport.com/device/K183247
Methodology: https://510kreport.com/methodology