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Data / Medical devices / China / Danyang Maxthai Medical Equipment Co., Ltd.

Danyang Maxthai Medical Equipment Co., Ltd.: FDA-registered device maker in Danyang City, Jiangsu, China, 1 510(k) clearance

Danyang Maxthai Medical Equipment Co., Ltd. is registered with the FDA (registration 3007019343) in Danyang City, Jiangsu, China. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 1, 2007. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3007019343
Address
Danyang Lianhu Industrial Park, Danyang City, Jiangsu, China, 212300
Owner or operator
Danyang Maxthai Medical Equipment Co., Ltd. (10026022)
Roles
Exporter to the US, Manufacturer
First device listed
May 30, 2008
Registered through
2026
Brand names listed
Bath Equipment, Chair; with Castor, E-Cart, Infusion Stand, Oxygen Regulator, Raiser, Commode & Shower Chair, Wheelchair

Devices it lists

DeviceProduct codeClassRoleSource
Adaptor, HygieneILS1Exporter to the US, Manufactureraccessdata.fda.gov
Cart, Emergency, Cardiopulmonary (Excluding Equipment)BZN1Exporter to the US, Manufactureraccessdata.fda.gov
Chair, With CastersINM1Exporter to the US, Manufactureraccessdata.fda.gov
Regulator, Pressure, Gas CylinderCAN1Exporter to the US, Manufactureraccessdata.fda.gov
Stand, InfusionFOX1Exporter to the US, Manufactureraccessdata.fda.gov
Walker, MechanicalITJ1Exporter to the US, Manufactureraccessdata.fda.gov
Wheelchair, MechanicalIOR1Exporter to the US, Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
March 1, 2007K070176MAXHEALTH MECHANICAL WHEELCHAIR, K1IORSubstantially EquivalentMaxhealth Corp.accessdata.fda.gov

Compare with other makers

Updated March 1, 2007. 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.