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Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.

3 FDA records filed under this company name, from 2019 to 2026, in microcurrent and ems (NFO, 1), light for wrinkles (OHS, 1), hair removal (OHT, 1).

Also filed with slightly different spelling: “Touchbeauty Beauty & Health ( Shenzhen ) Co., Ltd”. We group names that differ only in capitals, spacing or punctuation.

The applicant is the company that filed with FDA. It can be the brand you know or a manufacturer that makes devices sold under other brand names; the device name as filed often shows which. We don't merge different company names, so check the A–Z list for related entries.

Electrical stimulation for aesthetic use (microcurrent and EMS) (NFO, 1)

510(k) cleared

VITA Multi-Function Head Brush (TB-2343F, TB-2442F)

510(k) number
K260179
Applicant
Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.
Product code
NFO: Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Regulation
21 CFR 882.5890, Class II
FDA decision
Substantially Equivalent (SESE)
Received

Indications for use

Not quoted here. The page with this statement is a scanned image whose text was machine-read, so we can't vouch for it word for word. Read FDA's PDF, page 4.

LED and light devices for wrinkles (OHS, 1)

510(k) cleared

VITA Multi-Function Head Brush (TB-2443F, TB-2442AF, TB-2343F, TB-2442F)

510(k) number
K252053
Applicant
Touchbeauty Beauty & Health ( Shenzhen ) Co., Ltd
Product code
OHS: Light Based Over The Counter Wrinkle Reduction
Regulation
21 CFR 878.4810, Class II
FDA decision
Substantially Equivalent (SESE)
Received

Indications for use

Not quoted here. The statement contains words we couldn't confirm (a typo, run-together words or a reading error), and we don't correct FDA's text. Read FDA's PDF, page 4.

Laser and IPL hair removal (mostly over-the-counter; 1 record says prescription use) (OHT, 1)

510(k) cleared

IPL Hair Removal Device

510(k) number
K183217
Applicant
Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.
Product code
OHT: Light Based Over-The-Counter Hair Removal
Regulation
21 CFR 878.4810, Class II
FDA decision
Substantially Equivalent (SESE)
Received

Indications for use

Not quoted here. We couldn't find a clean, complete statement in FDA's PDF, so we don't quote one. Read FDA's PDF.