# K252618: IPL Hair Removal Device (I6 S1, I6 D1, I6 M1)

- Pathway: 510(k) (Traditional)
- Applicant: Alovea Healthcare Co., Ltd.
- Decided: Nov 14, 2025 after 87 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: 28 generations back to K950019 (1995). 92 ancestors in all.
No later device cites it as a predicate yet.
0 of 93 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K250171: IPL Hair Removal Device (BE965A, BE965B, BE965C), Shenzhen Yang WO Electronic Co., Ltd. (2025) Summary page 5.
- K241998: Ice Cooling IPL Hair Removal Device (UI20 DB, UI20 RE, UI20 GP, UI20 PW, UI20S DB, UI20S RE, UI20S PW, UI20S GP,UI20 WH, UI20 GR, UI20 BS, UI20 MP, UI20 BL, UI20 PN, UI20 BR, UI20WG, UI20S WH, UI20S GR, UI20S BS, UI20S MP), Shenzhen Ulike Smart Electronics Co., Ltd. (2024) Summary page 5.

## Indications for use
The IPL 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/K252618
Methodology: https://510kreport.com/methodology