# K203510: IPL Hair removal

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Weikai Technology Co.,Ltd
- Decided: Feb 26, 2021 after 88 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: 20 generations back to K950019 (1995). 58 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 60 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K192432: IPL Home Use Hair Removal Device Model (s): D-1128, D-1103, D-1119, D-1129, D-1130, Shenzhen Bosidin Technology Co., Ltd. (2019) Summary page 4.
- K161428: PerfectSmooth, Shen Zhen Cosbeauty Co., Ltd. (2017) Summary page 4.
- K160968: iPulse SmoothSkin Gold Hair Removal Device, Cyden Limited (2016) Summary page 4.

## Most influential descendants
- K213830: Home use hair removal device, model: Precise Touch Pro (2022), 0 descendants of its own

## Indications for use
IPL Hair removal is an over-the-counter device intended for removal of unwanted body hair and/or facial hair.

Source page: https://510kreport.com/device/K203510
Methodology: https://510kreport.com/methodology