# K250131: IPL Hair Removal Device (M8011, M8012, M8013, M8015, M8021, M8022, M8023, M8025, M7011, M7012, M7021, M7023)

- Pathway: 510(k) (Traditional)
- Applicant: Mustech Electronics Co., Limited
- Decided: Mar 19, 2025 after 61 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). 64 ancestors in all.
No later device cites it as a predicate yet.
0 of 65 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K232575: Hair Removal Device, Model (s): R2815-G Pro, R2815-G, Shenzhen Jianchao Intelligent Technology Co., Ltd. (2023) 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
IPL Hair Removal Device is an over-the-counter device intended for removal of unwanted body hair and/or facial hair.

Source page: https://510kreport.com/device/K250131
Methodology: https://510kreport.com/methodology