Data / Medical devices / China / Ming Fai Industrial (shenzhen) Co. Ltd.

Ming Fai Industrial (shenzhen) Co. Ltd.: FDA-registered device maker in SHENZHEN Guangdong, China, 3 510(k) clearances

Name: Ming Fai Industrial (shenzhen) Co. Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Ming Fai Industrial (shenzhen) Co. Ltd. is registered with the FDA (registration 9710018) in SHENZHEN Guangdong, China. It lists 17 device types. The FDA files 3 510(k) clearances under its listings, the newest dated September 18, 2001. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number: 9710018
FEI number: 3003340745
Address: Ming Fai Industrial Estate BAINIKENG, PINGHU LONGGANG, SHENZHEN Guangdong, China, 518111
Owner or operator: Ming Fai Enterprise International Co., Ltd. (9035380)
Roles: Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed: April 30, 1998
Registered through: 2027
Brand names listed: 3-Ply Disposable Face Mask, ADHESIVE BANDAGE, Bag Decanter, Bottle Decanter, COTTON SWAB, Cotton ball / Cotton pad, DENTAL FLOSS, Drape Surgical and more

Devices it lists

Device	Product code	Class	Role	Source
Applicator, Absorbent Tipped, Non-Sterile	KXF	1	Contract manufacturer, Repackager or relabeler	accessdata.fda.gov
Bedding, Disposable, Medical	KME	1	Contract manufacturer, Repackager or relabeler	accessdata.fda.gov
Container, I.V.	KPE	2	Contract manufacturer	accessdata.fda.gov
Drape, Surgical, Antimicrobial	KKX	2	Contract manufacturer, Repackager or relabeler	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	Contract manufacturer	accessdata.fda.gov
Fiber, Medical, Absorbent	FRL	1	Contract manufacturer	accessdata.fda.gov
Floss, Dental	JES	1	Repackager or relabeler	accessdata.fda.gov
Media, Coupling, Ultrasound	MUI	2	Contract manufacturer	accessdata.fda.gov
Microscope, Operating & Accessories, Ac-Powered, Ophthalmic	HRM	1	Contract manufacturer	accessdata.fda.gov
Operating Room Accessories Table Tray	FWZ	1	Contract manufacturer, Repackager or relabeler	accessdata.fda.gov
Protector, Skin Pressure	FMP	1	Repackager or relabeler	accessdata.fda.gov
Set, I.V. Fluid Transfer	LHI	2	Contract manufacturer	accessdata.fda.gov
Stretcher, Patient Restraint	NZD	1	Contract manufacturer	accessdata.fda.gov
System, X-Ray, Fluoroscopic, Image-Intensified	JAA	2	Contract manufacturer, Repackager or relabeler	accessdata.fda.gov
Tape And Bandage, Adhesive	KGX	1	Repackager or relabeler	accessdata.fda.gov
Toothbrush, Manual	EFW	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Transducer, Ultrasonic, Diagnostic	ITX	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, 2001	K012168	ADVANCE MEDICAL DESIGNS FLUID POUCH	KKX	Substantially Equivalent	Advance Medical Designs, Inc.	accessdata.fda.gov
January 26, 2001	K003670	PATIENT DRAPE, SURGICAL	KKX	Substantially Equivalent	Advance Medical Designs, Inc.	accessdata.fda.gov
April 9, 1985	K850959	EQUIPMENT SNAP KOVERS	JAA	Substantially Equivalent	Advance Medical Designs, Inc.	accessdata.fda.gov

Compare with other makers

Updated September 18, 2001. 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.