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Zhejiang Excellent United Medical Technology Co.,ltd: FDA-registered device maker in Jinhua Zhejiang, China, 1 510(k) clearance

Name: Zhejiang Excellent United Medical Technology Co.,ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Zhejiang Excellent United Medical Technology Co.,ltd is registered with the FDA (registration 3038637162) in Jinhua Zhejiang, China. It lists 24 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 31, 2024. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number: 3038637162
Address: Room 602, 6th Floor, Unit 1, No.3 Wenhua Road, Choujiang Street, Yiwu City, Jinhua Zhejiang, China, 322000
Owner or operator: ZHEJIANG EXCELLENT UNITED MEDICAL TECHNOLOGY CO.,LTD (10093575)
Roles: Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler
First device listed: June 5, 2025
Registered through: 2026
Brand names listed: Adhesive Bandage; Blister Heel Bandages, Gel Bandages; BP CHIN BLEMISH PATCH;, Adhesive Eye Pad; Sterile Eye Pad, Adhesive Island Dressing; Blemish Patch, Adhesive Tape Remover Pad, Alcohol Cleaning Pads; Alcohol Prep Pad; Antiseptic Povidone Iodine Prep Pad;, Anti-Bacterial Bandage, BP NOSE BLEMISH PATCH; Medical Tape; Retention Tape; Silver Bandages; TP Reversible Tough Wrap; Wound Plaster, BZK Antiseptic Swab/Antiseptic Cleaning Wipes (Sting Free), Soap Wipe and more

Devices it lists

Device	Product code	Class	Role	Source
Anaerobic Box Glove	JTM	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Apparatus, Suction, Operating-Room, Wall Vacuum Powered	GCX	2	Contract manufacturer, Exporter to the US, Manufacturer	accessdata.fda.gov
Applicator, Absorbent Tipped, Non-Sterile	KXF	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Bandage, Elastic	FQM	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Bedding, Disposable, Medical	KME	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Container, Specimen Mailer And Storage, Non-Sterile	NNK	1	Exporter to the US, Repackager or relabeler	accessdata.fda.gov
Degreaser, Skin, Surgical	KOY	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Disinfectant, Medical Devices	LRJ	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Dispenser, Solid Medication	NXB	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Dressing, Wound, Drug	FRO	U	Exporter to the US	accessdata.fda.gov
Dressing, Wound, Hydrophilic	NAC	1	Exporter to the US, 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	accessdata.fda.gov
First Aid Kit With Drug	LRR	N	Contract manufacturer, Exporter to the US, Manufacturer	accessdata.fda.gov
First Aid Kit Without Drug	OHO	1	Contract manufacturer, Exporter to the US, Manufacturer	accessdata.fda.gov
Forceps	HTD	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Gauze / Sponge,Nonresorbable For External Use	NAB	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Instrument, Surgical, Disposable	KDC	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Pack, Hot Or Cold, Disposable	IMD	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Pad, Eye	HMP	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Scissors, General, Surgical	LRW	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Sling, Arm	ILI	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Tape And Bandage, Adhesive	KGX	1	Exporter to the US, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Tourniquet, Nonpneumatic	GAX	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Tray, Surgical, Instrument	FSM	1	Exporter to the US, 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
May 31, 2024	K232333	Anti-bacterial bandage	FRO	Substantially Equivalent	Jinhua Jingdi Medical Supplies Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated May 31, 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.