# K212771: LightStim Elipsa

- Pathway: 510(k) (Traditional)
- Applicant: Led Intellectual Properties, LLC
- Decided: Jan 26, 2022 after 148 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). 123 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 125 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K203214: DemarkQ WOW, DemarkQ POP, Shenzhen Kaiyan Medical CO, Ltd. (2021) Summary page 4.
- K183708: Poly Clear, Medtek Skincare, LLC (2019) Summary page 4.
- K150098: LightStim Professional 2-Panel Light, Led Intellectual Properties, LLC (2015) Summary page 4.

## Most influential descendants
- K261473: Chromix (2026), 0 descendants of its own

## Indications for use
The LightStim Elipsa is a LED light therapy device which uses specific wavelengths of light, produced by light emitting diodes (LEDs). It is intended to emit energy in the red and infrared region of the light spectrum to provide treatment for full face wrinkles. The blue and red light spectrum is intended for the treatment of mild to moderate inflammatory acne.

Source page: https://510kreport.com/device/K212771
Methodology: https://510kreport.com/methodology