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Shenzhen Bway Tech Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance

Name: Shenzhen Bway Tech Co., Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Shenzhen Bway Tech Co., Ltd. is registered with the FDA (registration 3016879560) in Shenzhen Guangdong, China. It lists 10 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 7, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3016879560
Address: 1709, Yunhua Times, Haoxiang Road, Bogang Community Shajing Street, Bao'an District, Shenzhen Guangdong, China, 518104
Owner or operator: Shenzhen Bway Tech Co., Ltd. (10076975)
Roles: Contract manufacturer, Exporter to the US, Manufacturer
First device listed: August 6, 2020
Registered through: 2026
Brand names listed: AcuPoint acupressure mat and pillow set, Compression Sleeve, Facial cleansing brush, J03, Knee Massager, LED Light Therapy Mask, Manual Massage Ball, Massage Gun,Vibrating Massage Ball,Velocity Ball, Massager with cold&hot massage heades and more

Devices it lists

Device	Product code	Class	Role	Source
Bedding, Disposable, Medical	KME	1	Contract manufacturer, Exporter to the US, Manufacturer	accessdata.fda.gov
Brush, Dermabrasion, Powered	GFE	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Cold Pack And Vibrating Massager	PHW	1	Contract manufacturer, Exporter to the US, Manufacturer	accessdata.fda.gov
Lamp, Infrared, Therapeutic Heating	ILY	2	Exporter to the US	accessdata.fda.gov
Light Based Over The Counter Wrinkle Reduction	OHS	2	Exporter to the US	accessdata.fda.gov
Massager, Therapeutic, Electric	ISA	1	Contract manufacturer, Exporter to the US, Manufacturer	accessdata.fda.gov
Massager, Therapeutic, Manual	LYG	1	Contract manufacturer, Exporter to the US, Manufacturer	accessdata.fda.gov
Over-The-Counter Powered Light Based Laser For Acne	OLP	2	Exporter to the US	accessdata.fda.gov
Pack, Hot Or Cold, Reusable	IME	1	Contract manufacturer, Exporter to the US, Manufacturer	accessdata.fda.gov
Support, Patient Position	CCX	1	Contract manufacturer, Exporter to the US, 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
August 7, 2025	K251667	LED Light Therapy Mask (M01, M02, M06, M07, M08, M09)	OHS	Substantially Equivalent	Shenzhen Liyoutong Technology Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated August 7, 2025. 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.