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Netop Industrial Company Limited: FDA-registered device maker in Dongguan Guangdong, China, 5 510(k) clearances

Name: Netop Industrial Company Limited FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Netop Industrial Company Limited is registered with the FDA (registration 3007543044) in Dongguan Guangdong, China. It lists 15 device types. The FDA files 5 510(k) clearances under its listings, the newest dated April 19, 2024. Registered through 2027. FDA data exported November 3, 2026.

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FDA registration number: 3007543044
Address: No.1, Muling Street, Gangzi Village, Changping Town, Dongguan Guangdong, China, 523571
Owner or operator: Netop Industrial Company Limited (10058654)
Roles: Contract manufacturer, Manufacturer
First device listed: October 18, 2018
Registered through: 2027
Brand names listed: #1011 Medicine Dispenser - Rocket, #1012 Medicine Dispenser - Butterfly, Acne Purifier BC-001+, Baby Nasal Washer, MC-301, Beaute & Hee (Face Skincare Massager) BC-041A, Bite Healer(HC-510A,HC-510), Cure Trio MC-310 Android, Cure Trio MC-310 iOS and more

Devices it lists

Device	Product code	Class	Role	Source
Clinical Electronic Thermometer	SDV	2	Manufacturer	accessdata.fda.gov
Dispenser, Liquid Medication	KYX	1	Contract manufacturer	accessdata.fda.gov
Exerciser, Non-Measuring	ION	1	Manufacturer	accessdata.fda.gov
Irrigator, Powered Nasal	KMA	1	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
Over-The-Counter Powered Light Based Laser For Acne	OLP	2	Manufacturer	accessdata.fda.gov
Pad, Heating, Powered	IRT	2	Manufacturer	accessdata.fda.gov
Stimulator, Electrical, Non-Implantable, For Incontinence	KPI	2	Manufacturer	accessdata.fda.gov
Stimulator, Electrical, Transcutaneous, For Arthritis	NYN	2	Manufacturer	accessdata.fda.gov
Stimulator, Muscle, Powered	IPF	2	Manufacturer	accessdata.fda.gov
Stimulator, Muscle, Powered, For Muscle Conditioning	NGX	2	Manufacturer	accessdata.fda.gov
Stimulator, Nerve, Transcutaneous, For Pain Relief	GZJ	2	Manufacturer	accessdata.fda.gov
Stimulator, Nerve, Transcutaneous, Over-The-Counter	NUH	2	Manufacturer	accessdata.fda.gov
Stimulator, Neuromuscular, External Functional	GZI	2	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
April 19, 2024	K233046	Electrical Neuromuscular Stimulator, Cure Trio	GZJ	Substantially Equivalent	Oriental Inspiration Limited	accessdata.fda.gov
April 13, 2022	K213133	Keffort (MC-100, MC-100A)	KPI	Substantially Equivalent	Oriental Inspiration Limited	accessdata.fda.gov
December 22, 2021	K212285	Electrical Neuromuscular Stimulator (Cure Trio MC-310 iOS, Cure Trio MC-310 Android)	NUH	Substantially Equivalent	Oriental Inspiration Limited	accessdata.fda.gov
May 3, 2017	K170269	Hee HR Mini	OHT	Substantially Equivalent	Oriental Inspiration Limited	accessdata.fda.gov
April 25, 2017	K170260	BC-001+ Acne Purifier	OLP	Substantially Equivalent	Oriental Inspiration Limited	accessdata.fda.gov

Compare with other makers

Updated April 19, 2024. 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.