Data / Medical devices / China / Jiangsu Weikang Jiejing Medical Apparatus Co., Ltd.

Jiangsu Weikang Jiejing Medical Apparatus Co., Ltd.: FDA-registered device maker in Shuyang Jiangsu, China, 2 510(k) clearances

Name: Jiangsu Weikang Jiejing Medical Apparatus Co., Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Jiangsu Weikang Jiejing Medical Apparatus Co., Ltd. is registered with the FDA (registration 3010594263) in Shuyang Jiangsu, China. It lists 18 device types. The FDA files 2 510(k) clearances under its listings, the newest dated January 8, 2015. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number: 3010594263
Address: #18 Wenzhou Road Economical Development District, Shuyang Jiangsu, China, 223600
Owner or operator: Jiangsu Weikang Jiejing Medical Apparatus Co., Ltd. (10045306)
Roles: Contract manufacturer, Manufacturer
First device listed: November 5, 2013
Registered through: 2026
Brand names listed: Cannula, Nasal, Oxygen, Conductive clear tube, Connectin Tube, Connecting Tubing, Drainage Bag, Drainage Tubes, Endotracheal Tube Stylet, Gastrointestinal Tube And Accessories, Non-breathing Mask, High Concentration and more

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Catheter	KGZ	1	Manufacturer	accessdata.fda.gov
Cannula, Nasal, Oxygen	CAT	1	Manufacturer	accessdata.fda.gov
Catheter And Tip, Suction	JOL	2	Contract manufacturer	accessdata.fda.gov
Catheters, Suction, Tracheobronchial	BSY	1	Contract manufacturer	accessdata.fda.gov
Collector, Urine, (And Accessories) For Indwelling Catheter	KNX	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Drain, Tee (Water Trap)	BYH	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Mask, Oxygen	BYG	1	Manufacturer	accessdata.fda.gov
Mask, Oxygen, Low Concentration, Venturi	BYF	1	Manufacturer	accessdata.fda.gov
Mask, Oxygen, Non-Rebreathing	KGB	1	Manufacturer	accessdata.fda.gov
Nebulizer (Direct Patient Interface)	CAF	2	Manufacturer	accessdata.fda.gov
Stylet, Tracheal Tube	BSR	1	Manufacturer	accessdata.fda.gov
Syringe, Irrigating (Non Dental)	KYZ	1	Manufacturer	accessdata.fda.gov
Trap, Sterile Specimen	BYZ	2	Manufacturer	accessdata.fda.gov
Tube, Aspirating, Flexible, Connecting	BYY	2	Contract manufacturer	accessdata.fda.gov
Tube, Tracheal (W/Wo Connector)	BTR	2	Manufacturer	accessdata.fda.gov
Tubes, Gastrointestinal (And Accessories)	KNT	2	Contract manufacturer	accessdata.fda.gov
Tubing, Noninvasive	GAZ	2	Contract manufacturer	accessdata.fda.gov
Tubing, Pressure And Accessories	BYX	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
January 8, 2015	K140237	DISPOSABLE NEBULIZER SET	CAF	Substantially Equivalent	Suzhou Weikang Medical Apparatus Co., Ltd.	accessdata.fda.gov
December 18, 2014	K140228	DISPOSABLE TRACHEAL TUBE	BTR	Substantially Equivalent	Suzhou Weikang Medical Apparatus Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated January 8, 2015. 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.