# K261705: Hair Removal Device (R3C16-G Pro, R3C16-V Pro)

- Pathway: 510(k) (Special)
- Applicant: Shenzhen Jianchao Intelligent Technology Co., Ltd.
- Decided: Aug 10, 2026 after 80 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: 26 generations back to K950019 (1995). 70 ancestors in all.
No later device cites it as a predicate yet.
0 of 71 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K242710: Hair Removal Device (R3C16-P, R3C16-W, R3C16-G, R3C16-P Pro, R3C16-W Pro, R3C16-G Pro, R3505-W, R3505-B, R3505-W Pro, R3505-B Pro), Shenzhen Jianchao Intelligent Technology Co., Ltd. (2024) Summary page 6.
- K241881: IPL Hair Removal Device (JM-843, JM-865, JM-638), Shenzhen Junmei Technology Co., Ltd. (2024) Summary page 6.

## Indications for use
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/K261705
Methodology: https://510kreport.com/methodology