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Touchbeauty Beauty & Health (shenzhen) Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 4 510(k) clearances

Name: Touchbeauty Beauty & Health (shenzhen) Co., Ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Touchbeauty Beauty & Health (shenzhen) Co., Ltd is registered with the FDA (registration 3010027944) in Shenzhen Guangdong, China. It lists 17 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 3, 2026. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number: 3010027944
Address: 7/F, Marina Bay Centre A, South of Xinhua Road, Bao'an Centre Area, Xin'an Street Bao'an District, Shenzhen Guangdong, China, 518100
Owner or operator: TOUCHBEAUTY BEAUTY & HEALTH ( SHENZHEN ) CO., LTD. (10056661)
Roles: Manufacturer
First device listed: January 1, 2018
Registered through: 2026
Brand names listed: Blackhead Remover, Body Massager: TB-1796, Electric Toothbrush, Eye massager: TB-1883, Facial Cleanser,Electric Facial Cleanser Set, GLAM LED Facial Mask TB-2386F, Graphene FIR Helmet TB-2546, IPL Goggles and more

Devices it lists

Device	Product code	Class	Role	Source
Brush, Dermabrasion, Powered	GFE	1	Manufacturer	accessdata.fda.gov
Device, Pressure Applying	KNM	1	Manufacturer	accessdata.fda.gov
Instrument, Surgical, Sonic And Accessory/Attachment	JDX	2	Manufacturer	accessdata.fda.gov
Lamp, Infrared, Therapeutic Heating	ILY	2	Manufacturer	accessdata.fda.gov
Laser, Comb, Hair	OAP	2	Manufacturer	accessdata.fda.gov
Light Based Over The Counter Wrinkle Reduction	OHS	2	Manufacturer	accessdata.fda.gov
Light Based Over-The-Counter Hair Removal	OHT	2	Manufacturer	accessdata.fda.gov
Massager, Therapeutic, Electric	ISA	1	Manufacturer	accessdata.fda.gov
Massager, Therapeutic, Manual	LYG	1	Manufacturer	accessdata.fda.gov
Over-The-Counter Powered Light Based Laser For Acne	OLP	2	Manufacturer	accessdata.fda.gov
Pad, Heating, Powered	IRT	2	Manufacturer	accessdata.fda.gov
Powered Laser Surgical Instrument	GEX	2	Manufacturer	accessdata.fda.gov
Powered Light Based Non-Laser Surgical Instrument With Thermal Effect	ONF	2	Manufacturer	accessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	HOY	1	Manufacturer	accessdata.fda.gov
Stimulator, Transcutaneous Electrical, Aesthetic Purposes	NFO	2	Manufacturer	accessdata.fda.gov
Syringe, Irrigating (Dental)	EIB	1	Manufacturer	accessdata.fda.gov
Toothbrush, Powered	JEQ	1	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
June 3, 2026	K260179	VITA Multi-Function Head Brush (TB-2343F, TB-2442F)	NFO	Substantially Equivalent	Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.	accessdata.fda.gov
October 27, 2025	K252053	VITA Multi-Function Head Brush (TB-2443F, TB-2442AF, TB-2343F, TB-2442F)	OHS	Substantially Equivalent	Touchbeauty Beauty & Health ( Shenzhen ) Co., Ltd	accessdata.fda.gov
August 29, 2025	K251727	GLAM LED Facial Mask (TB-2386F)	GEX	Substantially Equivalent	Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.	accessdata.fda.gov
February 15, 2019	K183217	IPL Hair Removal Device	OHT	Substantially Equivalent	Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated June 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.