Data / Medical devices / China / Shenzhen Eyco Technology Co.,ltd

Shenzhen Eyco Technology Co.,ltd: FDA-registered device maker in Shenzhen Guangdong, China, 2 510(k) clearances

Name: Shenzhen Eyco Technology Co.,ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Shenzhen Eyco Technology Co.,ltd is registered with the FDA (registration 3017555752) in Shenzhen Guangdong, China. It lists 27 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 5, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3017555752
Address: 2 / F, Building 1, Jiashitai Science Park, 164# Fengtang Avenue, Fuhai Street, Baoan District, Shenzhen Guangdong, China, 518103
Owner or operator: Shenzhen Eyco Technology Co.,Ltd (10092931)
Roles: Manufacturer
First device listed: March 7, 2025
Registered through: 2026
Brand names listed: Brand: Pure Daily Care LUMA Light LED Therapy Facial Mask ( Model:E43 ); Luma Skin Therapy Wand (Model: E56 ), Cold massager, Cosmetic Products, Electric tooth brush, Electronic beauty device, Eye mask (Model:e200a ), Eye pen massager, Facial cleaning brush and more

Devices it lists

Device	Product code	Class	Role	Source
Adaptor, Grooming	ILW	1	Manufacturer	accessdata.fda.gov
Adaptor, Hygiene	ILS	1	Manufacturer	accessdata.fda.gov
Adaptor, Recreational	ILT	1	Manufacturer	accessdata.fda.gov
Analyzer, Rigidity	GZM	2	Manufacturer	accessdata.fda.gov
Brush, Dermabrasion, Manual	GED	1	Manufacturer	accessdata.fda.gov
Brush, Dermabrasion, Powered	GFE	1	Manufacturer	accessdata.fda.gov
Cold Pack And Vibrating Massager	PHW	1	Manufacturer	accessdata.fda.gov
Detectors And Removers, Lice, (Including Combs)	LJL	1	Manufacturer	accessdata.fda.gov
Device, Pressure Applying	KNM	1	Manufacturer	accessdata.fda.gov
Epilator, High Frequency, Tweezer-Type	KCX	1	Manufacturer	accessdata.fda.gov
Exerciser, Powered	BXB	1	Manufacturer	accessdata.fda.gov
Headlamp, Operating, Battery-Operated	HPP	1	Manufacturer	accessdata.fda.gov
Humidifier, Non-Direct Patient Interface (Home-Use)	KFZ	1	Manufacturer	accessdata.fda.gov
Lamp, Infrared, Therapeutic Heating	ILY	2	Manufacturer	accessdata.fda.gov
Led Light Source	NTN	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
Pack, Hot Or Cold, Water Circulating	ILO	2	Manufacturer	accessdata.fda.gov
Protector, Skin Pressure	FMP	1	Manufacturer	accessdata.fda.gov
Source, Carrier, Fiberoptic Light	EQH	1	Manufacturer	accessdata.fda.gov
Static Electricity-Emitting Device, Cosmetic Use	NZF	N	Manufacturer	accessdata.fda.gov
Toothbrush, Powered	JEQ	1	Manufacturer	accessdata.fda.gov
Unit, Heating, Powered	IRQ	1	Manufacturer	accessdata.fda.gov
Vibrator, Therapeutic	IRO	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
February 5, 2025	K243555	LED light therapy mask (E43, E32, E49B, E49C, E100B, E100C, E103B, E104B, E106A, E108A)	OLP	Substantially Equivalent	Shenzhen Eyco Technology Co., Ltd.	accessdata.fda.gov
July 10, 2024	K240016	IPL Hair Removal Device (YT01,YT02,YT03,YT04)	OHT	Substantially Equivalent	Shenzhen Jianrong Biomedical Electronics Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated February 5, 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.