# K230042: Q-Rejuvalight Pro Facewear (Model: P19-0023)

- Pathway: 510(k) (Traditional)
- Applicant: Light Tree Ventures Europe B.V.
- Decided: Apr 28, 2023 after 112 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: 18 generations back to K943450 (1995). 124 ancestors in all.
9 later devices descend from it; 7 cite it directly.
0 of 134 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183247: dpl Faceware, Led Technologies, Inc. (2019) Summary page 5.
- K230124: LUSTRE ClearSkin Renew Pro Facewear Mask (Model: PR4001), Light Tree Ventures Europe B.V. (2023). Cleared while this submission was under review Summary page 5.
- K171390: dpl II Panel, Led Technologies, Inc. (2017) Summary page 5.

## Most influential descendants
- 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
- K253135: LED Light Therapy Device (HLGMZ-3W-G1V1,HLGMZ-3W-G2V1,HLG-GJXJ-G1V1,HGMZ-2W-G1V1, HGMZ-2W-G2V1,MRD-GJXJ-G1V1.) (2025), 0 descendants of its own

## Indications for use
The Q-Rejuvalight Pro Facewear (Model: P19-0023) is an Over-the-Counter (OTC) device intended for treatment of wrinkles and mild to moderate inflammatory acne.

Source page: https://510kreport.com/device/K230042
Methodology: https://510kreport.com/methodology