# K211185: IPL Home Use Hair Removal Device

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.
- Decided: Dec 20, 2021 after 244 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.
8 later devices descend from it; 2 cite it directly.
0 of 67 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.
- K160968: iPulse SmoothSkin Gold Hair Removal Device, Cyden Limited (2016) Summary page 4.

## Most influential descendants
- K221001: IPL Home Use Hair Removal Device (2022), 6 descendants of its own
- K241881: IPL Hair Removal Device (JM-843, JM-865, JM-638) (2024), 1 descendant of its own
- K222316: IPL Hair Removal Device (2022), 1 descendant of its own
- K261705: Hair Removal Device (R3C16-G Pro, R3C16-V Pro) (2026), 0 descendants of its own
- K240583: IPL Home Use Hair Removal Device (D-1199, D-T099, D-T018, D-T019, D-T003B, D-T003W, D-T018Y, D-T019Y, D-1196B, D-1196W, D-1196C, D-1196C1, D-T099K, D-T099KW, D-T012, D-T012W) (2024), 0 descendants of its own

## 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/K211185
Methodology: https://510kreport.com/methodology