# K231215: IPL Hair Removal Device Model: Skin Expert Pro IPL 008, Skin Expert Pro IPL 008S

- Pathway: 510(k) (Traditional)
- Applicant: Zhongshan Qizhe Technology Co., Ltd.
- Decided: Jun 26, 2023 after 59 days
- Product code: OHT (Light Based Over-The-Counter Hair Removal)
- 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: 23 generations back to K950019 (1995). 63 ancestors in all.
No later device cites it as a predicate yet.
0 of 64 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183217: IPL Hair Removal Device, Touchbeauty Beauty & Health (Shenzhen) Co., Ltd. (2019) Summary page 5.
- K223928: Intense Pulsed Light (IPL) System, model: T023K, T023A, T023B, T023C, T023D, T023E, T021K, T021A, T001A, T001B, T001M, T001N, T011C, T016K, Shenzhen Fansizhe Science and Technology Co., Ltd. (2023) Summary page 5.

## Indications for use
The IPL Hair Removal device (Model: Skin Expert Pro IPL 008, Skin Expert Pro IPL 008S) is an Over the Counter device intended for the removal of unwanted body hair.

Source page: https://510kreport.com/device/K231215
Methodology: https://510kreport.com/methodology