# K223147: myLEDmask

- Pathway: 510(k) (Traditional)
- Applicant: Myblend
- Decided: May 14, 2023 after 221 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). 101 ancestors in all.
4 later devices descend from it; 3 cite it directly.
0 of 106 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 4.
- K140471: Pro X Otc 5, La Lumiere, LLC (2015) Summary page 4.
- K171323: Biophotas CELLUMA3, Biophotas, Inc. (2017) Summary page 4.
- K183671: LG Pra.L Derma Led Mask, Lg Electronics.Inc (2019) Summary page 4.

## Most influential descendants
- K241947: EnergyLounger (TY-01) (2025), 1 descendant of its own
- K260415: myLEDmask 2 (MJ-144) (2026), 0 descendants of its own
- K260688: Sculpt LED Belt (HY-150A/HY-150B/HY-200A/HY-200B/HY-420A/HY-200D/HY-200C) (2026), 0 descendants of its own
- K253279: Feather/numiere 05 06 07 (05) (2025), 0 descendants of its own

## Indications for use
myLEDmask is an over-the-counter device that is intended to emit energy in the visible and infrared region of the spectrum for use in the treatment of full-face wrinkles.

Source page: https://510kreport.com/device/K223147
Methodology: https://510kreport.com/methodology