Light Based Hair Removal Device

Shenzhen Meik Beauty Industry Co., Ltd.

Country / region:China (CN)Submission type:Traditional

Product code OHT· 21 CFR 878.4810

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Product code

OHT
21 CFR 878.4810

Predicate devices

3

Cited as predicate

0

Device details

FDA 510(k) registration fields

K number
K232846
Device name
Light Based Hair Removal Device
Country / region
China(CN)
Product code
OHT
Device class
Class 2
Regulation number
21 CFR 878.4810
Date received
2023-09-14
Decision date
2023-12-07
Submission type
Traditional
Technology type
Other(AI inferred)
Clinical applications
Body
Primary application
Body
Classification source
AI classified

Indications for Use

Light Based Hair Removal Device is an over-the-counter device intended for removal of unwanted body hair.

Intended Use

Light Based Hair Removal Device is an over-the-counter device intended for removal of unwanted body hair.

Device Description

The Light Based Hair Removal Device is a personal, light-based, hair reduction device intended to be sold over-the-counter directly to the end user. The device provides hair reduction using Intense Pulsed Light (IPL) technology, and it works below the skin's surface and does not involve any cutting or pulling, reducing hair growth with minimal pain. The Light Based Hair Removal Device is only powered by the external power adapter and its IPL emission activation is by finger switch. The device contains a Xenon lamp and its built-in skin sensor to detect appropriate skin contact. If the device is not properly and fully applied to the treated skin, the device will not emit the light pulse. There are A113, A112, and AM001 three models in this application. Their work principle, function, intended use, structure, and composition are the same, with differences being product appearance, size, and energy output density are slight differences, but these parameters are within the.

Summary parsed at:2026-06-11 04:42:42 UTC

Predicate devices

3

K232846 references 3 predicate/reference devices

Cited as predicate

0

No later 510(k)s cite this device yet

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