Q-Rejuvalight Pro Facewear (Model: P19-0023) (K230042)
Description
Q-Rejuvalight Pro Facewear (Model: P19-0023) by Light Tree Ventures Europe B.V., an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K230042
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Q-Rejuvalight Pro Facewear (Model: P19-0023) (K230042) cites 3 predicate devices and is itself cited by 3 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K230124 | LUSTRE ClearSkin Renew Pro Facewear Mask(Model: PR4001) | Light Tree Ventures Europe B.V. | 2023 |
| K183247 | dpl Faceware | Led Technologies, Inc. | 2019 |
| K171390 | dpl II Panel | Led Technologies, Inc. | 2017 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K251588 | LED Light Therapy Mask (FCM902, FCM905, FCM906, FCM908, 11-... | Shenzhen Fittop Health Technology C... | 2025 |
| K251871 | FEATHER 01 02 03 04 (Model:01) | Heat IN A Click, LLC | 2025 |
| K243330 | LYMA Laser PRO | Lyma Life , Ltd. | 2025 |
Trace the full predicate network for K230042
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.