Data / Medical devices / China / Suzhou Vicon Industrial Co., Ltd

Suzhou Vicon Industrial Co., Ltd: FDA-registered device maker in SUZHOU Jiangsu, China, 1 510(k) clearance

Name: Suzhou Vicon Industrial Co., Ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Suzhou Vicon Industrial Co., Ltd is registered with the FDA (registration 3006633581) in SUZHOU Jiangsu, China. It lists 13 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 17, 2002. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number: 3006633581
Address: 11 Shitian Road, Yangchenghu Town Xiangcheng District, SUZHOU Jiangsu, China, 215122
Owner or operator: SUZHOU VICON INDUSTRIAL CO., LTD. (9101979)
Roles: Contract manufacturer, Manufacturer
First device listed: May 23, 2007
Registered through: 2027
Brand names listed: ABD Pads, Abdominal Pad, Trauma Pad, BANDAGE, CAST, CAST PADDING, Compress Bandage; Compress Gauze Bandage; Krinkle Gauze Roll; Stopper Trauma Dressing, Dyna-Stopper Trauma Dressing Sterile, Eye Pad; Pad, Eye, Gauze; Rolled Gauze; Sterile First-aid Dressing Bandage, General Surgical Scissors, NON-ADHESIVE DRESSING and more

Devices it lists

Device	Product code	Class	Role	Source
Bandage, Cast	ITG	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Bandage, Elastic	FQM	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Dressing, Compression	MHW	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Dressing, Wound, Drug	FRO	U	Manufacturer	accessdata.fda.gov
Dressing, Wound, Hydrophilic	NAC	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Dressing, Wound, Occlusive	NAD	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
First Aid Kit Without Drug	OHO	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Gauze / Sponge,Nonresorbable For External Use	NAB	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Kit, Surgical Instrument, Disposable	KDD	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Pad, Eye	HMP	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Scissors, General, Surgical	LRW	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Sling, Arm	ILI	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Tape And Bandage, Adhesive	KGX	1	Contract manufacturer, 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
October 17, 2002	K012816	DYNAREX IODOFORM PACKING STRIPS, MODELS 3411, 3412, 3413, 3414	FRO	Substantially Equivalent	Dynarex Corp.	accessdata.fda.gov

Compare with other makers

Updated October 17, 2002. 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.