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Data / Medical devices / China / Zhejiang Mateside Medical Devices Technology Co., Ltd

Zhejiang Mateside Medical Devices Technology Co., Ltd: FDA-registered device maker in Ningbo Zhejiang, China, 1 510(k) clearance

Zhejiang Mateside Medical Devices Technology Co., Ltd is registered with the FDA (registration 3016678950) in Ningbo Zhejiang, China. It lists 21 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 21, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3016678950
Address
Room 10-1, 10-2, 10-3, 10-4, Building 30, No. 300 Desheng Road, Zhanqi Town, Yinzhou District, Ningbo Zhejiang, China, 315100
Owner or operator
Zhejiang Mateside Medical Devices Technology Co., Ltd (10062787)
Roles
Contract manufacturer, Exporter to the US, Manufacturer
First device listed
March 8, 2020
Registered through
2026
Brand names listed
Anti-Tip Wheels, Anti-decubitus air mattress, Bath Lift, Electric Seat Lift, Electric Seat Lifter, Electric Rise Up Seat, Bathtub Transfer Bench, Transfer Bench, Sliding Shower Chair, Swivel Shower Chair, Shower Safety Seat, CABINET, TABLE AND TRAY, ANESTHESIA, Chair Lift, Disposable Underpads, Electric Home Bed and more

Devices it lists

DeviceProduct codeClassRoleSource
Adaptor, HygieneILS1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Bed, Ac-Powered Adjustable HospitalFNL2Exporter to the US, Manufactureraccessdata.fda.gov
Bed, ManualFNJ1Exporter to the US, Manufactureraccessdata.fda.gov
Bed, Therapeutic, Ac-Powered, Adjustable Home-UseLLI2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Chair And Table, MedicalKMN1Exporter to the US, Manufactureraccessdata.fda.gov
Chair, Adjustable, MechanicalINN1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Chair, Positioning, ElectricINO2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Chair, With CastersINM1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Device, Anti-Tip, WheelchairIMR1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Device, Patient Transfer, PoweredFRZ2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Device, Transfer, Patient, ManualFMR1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Exerciser, PoweredBXB1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Garment, Protective, For IncontinenceEYQ1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Lift, Patient, Ac-PoweredFNG2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Lift, Patient, Non-Ac-PoweredFSA1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Massager, Therapeutic, ElectricISA1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Mattress, Air Flotation, Alternating PressureFNM2Exporter to the US, Manufactureraccessdata.fda.gov
Orthosis, CervicalIQK1Exporter to the US, Manufactureraccessdata.fda.gov
System, Isokinetic Testing And EvaluationIKK2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Walker, MechanicalITJ1Contract manufacturer, Exporter 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
July 21, 2022K220671Manual WheelchairIORSubstantially EquivalentHebei Ruilangde Medical Equipment Technology Group Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated July 21, 2022. 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.