Data / Medical devices / China / Shenzhen Jie Zhong Lian Technology Co., Ltd.

Shenzhen Jie Zhong Lian Technology Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance

Name: Shenzhen Jie Zhong Lian Technology Co., Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Shenzhen Jie Zhong Lian Technology Co., Ltd. is registered with the FDA (registration 3023339107) in Shenzhen Guangdong, China. It lists 17 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 18, 2017. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number: 3023339107
Address: 5th Floor, Building 3, Xinyuan Zhichuang Valley, Tangwei Community, Fuhai Street, Baoan District, Shenzhen Guangdong, China, 518103
Owner or operator: Shenzhen Jie Zhong Lian Technology Co., Ltd. (10085347)
Roles: Contract manufacturer, Manufacturer
First device listed: June 7, 2022
Registered through: 2026
Brand names listed: Ankle massager:MZ-J01,MZ-J01A,MZ-J01B,MZ-1616, Blackhead removal device,MZ-BR01,MZ-BR02,MZ-BR03,MZ-BR04,MZ-050,MZ-1728,MZ-BR08, Body Gua Sha and Cupping Therapy:MZ-166A,MZ-XYT213,MZ-GS55,MZ-GS40,MZ-GS37,MZ-GS39,MZ-GS40, Derma Rolling System,MZ-A6,MZ-A6S, MZ-M8,MZ-M7, EMS beauty device:MZ-1607, MZ-HM206, EMS beauty device:MZ-F2,MZ-D818,MZ-DS8822,MZ-XGY025,MZ-BI09,MZ-BI22, EMS eye massager,MZ-LA005,MZ-1711,MZ-601,MZ-C507,MZ-XM002, Eye massager,MZ-EM4S,MZ-EM6S,MZ-EM8S,MZ-EM9A,MZ-EM10C,MZ-EM10A,ST-208,MZ-H9,MZ-Q7,MZ-EM203 and more

Devices it lists

Device	Product code	Class	Role	Source
Brush, Dermabrasion, Powered	GFE	1	Manufacturer	accessdata.fda.gov
Burr, Corneal, Battery Powered, Rust Ring Removal	OHW	1	Manufacturer	accessdata.fda.gov
Cleaner, Ultrasonic, Medical Instrument	FLG	1	Manufacturer	accessdata.fda.gov
Detectors And Removers, Lice, (Including Combs)	LJL	1	Manufacturer	accessdata.fda.gov
Device, Accessory, Cooling Plate For Tissue Embedding Station	MXT	1	Manufacturer	accessdata.fda.gov
Lamp, Infrared, Therapeutic Heating	ILY	2	Manufacturer	accessdata.fda.gov
Laser, Comb, Hair	OAP	2	Contract manufacturer	accessdata.fda.gov
Light Based Over The Counter Wrinkle Reduction	OHS	2	Contract manufacturer	accessdata.fda.gov
Light Based Over-The-Counter Hair Removal	OHT	2	Contract manufacturer	accessdata.fda.gov
Massager, Therapeutic, Electric	ISA	1	Manufacturer	accessdata.fda.gov
Massager, Vacuum, Radio Frequency Induced Heat	PBX	2	Manufacturer	accessdata.fda.gov
Pad, Heating, Powered	IRT	2	Manufacturer	accessdata.fda.gov
Stimulator, Electrical, Transcutaneous, For Arthritis	NYN	2	Contract manufacturer	accessdata.fda.gov
Stimulator, Muscle, Powered	IPF	2	Contract manufacturer	accessdata.fda.gov
Stimulator, Muscle, Powered, For Muscle Conditioning	NGX	2	Contract manufacturer	accessdata.fda.gov
Stimulator, Nerve, Transcutaneous, For Pain Relief	GZJ	2	Contract manufacturer	accessdata.fda.gov
Stimulator, Nerve, Transcutaneous, Over-The-Counter	NUH	2	Contract 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
September 18, 2017	K162828	Winback Back 3SE	PBX	Substantially Equivalent	Winback USA Corp	accessdata.fda.gov

Compare with other makers

Updated September 18, 2017. 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.