Data / Medical devices / China / Jiangsu Medplus Non-Woven Manufacturer Co.,ltd.

Jiangsu Medplus Non-Woven Manufacturer Co.,ltd.: FDA-registered device maker in Siyang Jiangsu, China, 1 510(k) clearance

Name: Jiangsu Medplus Non-Woven Manufacturer Co.,ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Jiangsu Medplus Non-Woven Manufacturer Co.,ltd. is registered with the FDA (registration 3017194442) in Siyang Jiangsu, China. It lists 21 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 10, 2021. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number: 3017194442
Address: No.217 East Wencheng Road, Economic Development Zone, Siyang, Jiangsu, 223700, China, Siyang Jiangsu, China, 223700
Owner or operator: Jiangsu Medplus Non-woven Manufacturer Co.,Ltd. (10074932)
Roles: Exporter to the US, Manufacturer
First device listed: June 2, 2020
Registered through: 2026
Brand names listed: Banded Bag, C-arm Drape, Camera Drape, Disposable Face Masks, Disposable Isolation Gowns, Disposable Shoe Covers, Disposable Surgical Caps, Disposable Surgical Drape and more

Devices it lists

Device	Product code	Class	Role	Source
Accessory, Surgical Apparel	LYU	1	Manufacturer	accessdata.fda.gov
Bag, Ice	KYR	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Bedding, Disposable, Medical	KME	1	Manufacturer	accessdata.fda.gov
Cap, Surgical	FYF	1	Manufacturer	accessdata.fda.gov
Cover, Shoe, Operating-Room	FXP	1	Manufacturer	accessdata.fda.gov
Drape, Adhesive, Aerosol	KGT	1	Manufacturer	accessdata.fda.gov
Drape, Microscope, Ophthalmic	HMW	2	Manufacturer	accessdata.fda.gov
Drape, Patient, Ophthalmic	HMT	2	Manufacturer	accessdata.fda.gov
Drape, Pure Latex Sheet, With Self-Retaining Finger Cot	EYX	2	Manufacturer	accessdata.fda.gov
Drape, Surgical, Ent	ERY	2	Manufacturer	accessdata.fda.gov
Drape, Surgical, Exempt	PUI	2	Manufacturer	accessdata.fda.gov
Drape, Urological, Disposable	EYY	2	Manufacturer	accessdata.fda.gov
Dress, Surgical	FYE	1	Manufacturer	accessdata.fda.gov
Gown, Examination	FME	1	Manufacturer	accessdata.fda.gov
Kit, Surgical Instrument, Disposable	KDD	1	Manufacturer	accessdata.fda.gov
Mask, Gas, Anesthetic	BSJ	1	Manufacturer	accessdata.fda.gov
Mask, Scavenging	KHA	1	Manufacturer	accessdata.fda.gov
Mask, Surgical	FXX	2	Manufacturer	accessdata.fda.gov
Non-Surgical Gown	OEA	1	Manufacturer	accessdata.fda.gov
Ring (Wound Protector), Drape Retention, Internal	KGW	2	Manufacturer	accessdata.fda.gov
Suit, Surgical	FXO	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
February 10, 2021	K202605	Standard Procedure Mask, Standard Surgical Mask	FXX	Substantially Equivalent	Jiangsu Medplus Non-Woven Manufacturer Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated February 10, 2021. 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.