# K252234: IPL Home Use Hair Removal Device (Models: FDA11, FDA12, FDA13, FDA14, FDA15, FDA16, FDA17, FDA18, FDA19, FDA20, FDA21S, FDA22S, FDA23S, FDA24S, FDA25, FDA26, FDA27, FDA28, FDA29S, FDA30S, FDA31S)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Qiaochengli Technology Co., Ltd.
- Decided: Oct 14, 2025 after 89 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: 25 generations back to K950019 (1995). 66 ancestors in all.
No later device cites it as a predicate yet.
0 of 67 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K221569: Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K, Shenzhen Fansizhe Science and Technology Co., Ltd. (2022) Summary page 5.
- K241120: Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S), Qiaocheng LI (Dongguan) Medical Instruments Co., Ltd. (2024) Summary page 5.

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

Source page: https://510kreport.com/device/K252234
Methodology: https://510kreport.com/methodology