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Ningbo Just Soon Industrial Limited: FDA-registered device maker in Ningbo Zhejiang, China, 1 510(k) clearance

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

Ningbo Just Soon Industrial Limited is registered with the FDA (registration 3011919098) in Ningbo Zhejiang, China. It lists 36 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 12, 2022. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number: 3011919098
Address: Room 402, 4th Floor, Building 1, No. 688, Jinda Road, Panhuo Street Yinzhou District, Ningbo,China, 315000, Ningbo Zhejiang, China, 315000
Owner or operator: NINGBO JUST SOON INDUSTRIAL LIMITED (10075118)
Roles: Exporter to the US, Manufacturer, Repackager or relabeler
First device listed: June 6, 2020
Registered through: 2026
Brand names listed: 4 in 1 Pill Splitter Organizer, Acupressure Foldable Foot Mat, Adult Incontinence Pad / Disposable Protective Garment for Incontinence, Animal Neck Massager, Anti-Snore Clips, Aromatherapy diffuser with essential oils included, Bath,Sitz,Nonpowered, Bug bite relief patches and more

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Wheelchair	KNO	1	Exporter to the US, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Adaptor, Dressing	ILD	1	Manufacturer	accessdata.fda.gov
Adaptor, Hygiene	ILS	1	Manufacturer	accessdata.fda.gov
Adhesive Backed Thermal Skin Patches	OMW	1	Manufacturer	accessdata.fda.gov
Aid, Transfer	IKX	1	Manufacturer	accessdata.fda.gov
Bath, Sitz, Nonpowered	KTC	1	Exporter to the US, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Cane	IPS	1	Manufacturer	accessdata.fda.gov
Cane, Safety Walk	KHY	1	Manufacturer	accessdata.fda.gov
Cleaner, Ultrasonic, Medical Instrument	FLG	1	Manufacturer	accessdata.fda.gov
Continuous Measurement Thermometer	FLL	2	Manufacturer	accessdata.fda.gov
Dilator, Nasal	LWF	1	Manufacturer	accessdata.fda.gov
Dressing, Compression	MHW	1	Manufacturer	accessdata.fda.gov
Dressing, Wound, Hydrophilic	NAC	1	Manufacturer	accessdata.fda.gov
Enema Kit	FCE	1	Manufacturer	accessdata.fda.gov
Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua	QKR	N	Exporter to the US, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Foot Wrap For Treating Restless Leg Syndrome Symptoms	OTX	1	Manufacturer	accessdata.fda.gov
Garment, Protective, For Incontinence	EYQ	1	Manufacturer	accessdata.fda.gov
Humidifier, Non-Direct Patient Interface (Home-Use)	KFZ	1	Manufacturer	accessdata.fda.gov
Inserter/Remover Contact Lens	KYE	1	Manufacturer	accessdata.fda.gov
Joint, Knee, External Brace	ITQ	1	Manufacturer	accessdata.fda.gov
Massager, Therapeutic, Electric	ISA	1	Manufacturer	accessdata.fda.gov
Massager, Therapeutic, Manual	LYG	1	Manufacturer	accessdata.fda.gov
Nasal Spray, Ent Delivery	KCO	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Orthosis, Cervical	IQK	1	Manufacturer	accessdata.fda.gov
Pack, Hot Or Cold, Disposable	IMD	1	Manufacturer	accessdata.fda.gov
Pack, Hot Or Cold, Reusable	IME	1	Manufacturer	accessdata.fda.gov
Pad, Heating, Powered	IRT	2	Exporter to the US, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Pad, Menstrual, Unscented	HHD	1	Manufacturer	accessdata.fda.gov
Pill Crusher/Cutter	OHY	1	Manufacturer	accessdata.fda.gov
Shield, Nipple	HFS	1	Manufacturer	accessdata.fda.gov
Spectacle, Magnifying	HOI	1	Manufacturer	accessdata.fda.gov
Stocking, Medical Support (For General Medical Purposes)	FQL	1	Manufacturer	accessdata.fda.gov
Table, Obstetrical, Ac-Powered (And Accessories)	HDD	2	Manufacturer	accessdata.fda.gov
Thermometer Kit	PXH	2	Exporter to the US, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Tips And Pads, Cane, Crutch And Walker	INP	1	Manufacturer	accessdata.fda.gov
Utensil, Eating	ILC	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
September 12, 2022	K220084	Infrared Forehead Thermometer	FLL	Substantially Equivalent	Qingdao Yasee Medical Device Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated September 12, 2022. 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.