Data / Medical devices / China / China (shenyang) Med-Land Imp/Exp Corp., Ltd.

China (shenyang) Med-Land Imp/Exp Corp., Ltd.: FDA-registered device maker in Shanghai, China, 2 510(k) clearances

Name: China (shenyang) Med-Land Imp/Exp Corp., Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

China (shenyang) Med-Land Imp/Exp Corp., Ltd. is registered with the FDA (registration 8043685) in Shanghai, China. It lists 32 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 16, 2011. Registered through 2026. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch China (shenyang) Med-Land Imp/Exp Corp., Ltd.

FDA registration number: 8043685
FEI number: 3011343761
Address: No#255 New Jinqiao Road, Room 513, Shanghai, China, 201206
Owner or operator: CHINA SHENYANG MED-LAND IMP/EXP CORP., LTD. (9003235)
Roles: Exporter to the US
First device listed: August 20, 1996
Registered through: 2026
Brand names listed: Absorbant Tipped Applicator, Cane, Color Change Thermometer, Contact Lens Case, Crutch, Elastic Bandage, Endoscope Cleaning Brushes, Face Mask and more

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Cleaning Brushes, For Endoscope	MNL	1	Exporter to the US	accessdata.fda.gov
Applicator, Absorbent Tipped, Non-Sterile	KXF	1	Exporter to the US	accessdata.fda.gov
Applicator, Absorbent Tipped, Sterile	KXG	1	Exporter to the US	accessdata.fda.gov
Attachment, Commode, Wheelchair	INB	1	Exporter to the US	accessdata.fda.gov
Bandage, Elastic	FQM	1	Exporter to the US	accessdata.fda.gov
Bottle, Hot/Cold Water	FPF	1	Exporter to the US	accessdata.fda.gov
Brake, Extension, Wheelchair	IMW	1	Exporter to the US	accessdata.fda.gov
Cabinet, Table And Tray, Anesthesia	BRY	1	Exporter to the US	accessdata.fda.gov
Cane	IPS	1	Exporter to the US	accessdata.fda.gov
Cannula, Nasal, Oxygen	CAT	1	Exporter to the US	accessdata.fda.gov
Cap, Surgical	FYF	1	Exporter to the US	accessdata.fda.gov
Case, Contact Lens	LRX	2	Exporter to the US	accessdata.fda.gov
Continuous Measurement Thermometer	FLL	2	Exporter to the US	accessdata.fda.gov
Coverslips, Microscope Slide	KES	1	Exporter to the US	accessdata.fda.gov
Crutch	IPR	1	Exporter to the US	accessdata.fda.gov
Depressor, Tongue, Non-Surgical	FMA	1	Exporter to the US	accessdata.fda.gov
Dispenser, Solid Medication	NXB	1	Exporter to the US	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	accessdata.fda.gov
Fast Green	HYC	1	Exporter to the US	accessdata.fda.gov
Pill Crusher/Cutter	OHY	1	Exporter to the US	accessdata.fda.gov
Protector, Skin Pressure	FMP	1	Exporter to the US	accessdata.fda.gov
Stages, Microscope	KEJ	1	Exporter to the US	accessdata.fda.gov
Stand, Infusion	FOX	1	Exporter to the US	accessdata.fda.gov
Stethoscope, Manual	LDE	1	Exporter to the US	accessdata.fda.gov
Syringe, Irrigating (Non Dental)	KYZ	1	Exporter to the US	accessdata.fda.gov
Table, Mechanical	INW	1	Exporter to the US	accessdata.fda.gov
Thermometer, Clinical Color Change	FQZ	1	Exporter to the US	accessdata.fda.gov
Thermometer, Clinical Mercury	FLK	2	Exporter to the US	accessdata.fda.gov
Toothbrush, Manual	EFW	1	Exporter to the US	accessdata.fda.gov
Tourniquet, Nonpneumatic	GAX	1	Exporter to the US	accessdata.fda.gov
Utensil, Homemaking	IKW	1	Exporter to the US	accessdata.fda.gov
Walker, Mechanical	ITJ	1	Exporter to the US	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
December 16, 2011	K112289	DISPOSABLE THERMOMETER COVERS AND SHEATHS	FLL	Substantially Equivalent	Kang ZE Industrial Co. Limited	accessdata.fda.gov
May 1, 2007	K071081	CONTACT LENS CASE	LRX	Substantially Equivalent	Ningbo Kaida Rubber and Plastic Technology Co., LT	accessdata.fda.gov

Compare with other makers

Updated December 16, 2011. 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.