Data / Medical devices / China / Meda Co., Ltd.

Meda Co., Ltd.: FDA-registered device maker in Tianjin, China, 6 510(k) clearances

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

Meda Co., Ltd. is registered with the FDA (registration 3006540052) in Tianjin, China. It lists 2 device types. The FDA files 6 510(k) clearances under its listings, the newest dated September 24, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3006540052
Address: F2C, F3D, F4C, F5, F6C, Building C2, Xinmao Science Skill Park Huayuan Industry Development Area, Tianjin, China, 300384
Owner or operator: MEDA CO., LTD. (10023915)
Roles: Contract manufacturer, Manufacturer
First device listed: April 9, 2012
Registered through: 2026
Brand names listed: MD-6000S

Devices it lists

Device	Product code	Class	Role	Source
System, Imaging, Pulsed Echo, Ultrasonic	IYO	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Transducer, Ultrasonic, Diagnostic	ITX	2	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
September 24, 2026	K260313	MD-6000S Bladder Scanner	IYO	Substantially Equivalent	MEDA Co., Ltd.	accessdata.fda.gov
November 18, 2021	K213070	MD-320W Ultrasound Biomicroscope	IYO	Substantially Equivalent	MEDA Co., Ltd.	accessdata.fda.gov
May 6, 2019	K182460	MD-6000P Bladder Scanner	IYO	Substantially Equivalent	MEDA Co., Ltd.	accessdata.fda.gov
November 17, 2015	K152318	MD-2300S Ultrasonic A/B Scanner for Ophthalmology	IYO	Substantially Equivalent	MEDA Co., Ltd.	accessdata.fda.gov
May 3, 2013	K121243	ULTRASONIC BIOMETER FOR OPHTHALMOLOGY ULTRASONIC PACHYMETER	IYO	Substantially Equivalent	MEDA Co., Ltd.	accessdata.fda.gov
March 23, 2012	K113304	BLADDER SCANNER	IYO	Substantially Equivalent	MEDA Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated September 24, 2026. 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.