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Data / Medical devices / China / Mobility Source Medical Technology Co., Ltd.

Mobility Source Medical Technology Co., Ltd.: FDA-registered device maker in Foshan Guangdong, China, 1 510(k) clearance

Mobility Source Medical Technology Co., Ltd. is registered with the FDA (registration 3016734231) in Foshan Guangdong, China. It lists 26 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 14, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3016734231
Address
160 Heheng Road, Yanghe Town, Gaoming District, Foshan Guangdong, China, 528513
Owner or operator
Mobility Source Medical Technology Co., Ltd. (10063560)
Roles
Contract manufacturer, Exporter to the US, Manufacturer
First device listed
March 21, 2020
Registered through
2026
Brand names listed
Backrest, Bedpan, Commode Chair, shower chair, shower commode chair, Counter, sponge, surgical, Nail clipper, PU Rotating Seat for Bath Lift, Sofa Assist Rail, Step Stool with Handrail,Stand Assist, adjustable step for bath,bedside adjustable step stool and more

Devices it lists

DeviceProduct codeClassRoleSource
Adaptor, HygieneILS1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Adult Portable Bed Rails For Medical PurposesQTC1Contract manufacturer, Manufactureraccessdata.fda.gov
Aid, TransferIKX1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Apparatus, Traction, Non-PoweredHST1Contract manufacturer, Manufactureraccessdata.fda.gov
Attachment, Commode, WheelchairINB1Contract manufacturer, Manufactureraccessdata.fda.gov
Bed, ManualFNJ1Contract manufacturer, Manufactureraccessdata.fda.gov
BedpanFOB1Contract manufacturer, Manufactureraccessdata.fda.gov
CaneIPS1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Chair And Table, MedicalKMN1Contract manufacturer, Manufactureraccessdata.fda.gov
Chair, Adjustable, MechanicalINN1Contract manufacturer, Manufactureraccessdata.fda.gov
Chair, With CastersINM1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Collector, Urine, Powered, Non Indwelling CatheterNZU1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Counter, Sponge, SurgicalLWH1Contract manufacturer, Manufactureraccessdata.fda.gov
CrutchIPR1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Cushion, WheelchairIMP1Contract manufacturer, Manufactureraccessdata.fda.gov
Cutter, SurgicalFZT1Contract manufacturer, Manufactureraccessdata.fda.gov
Gauze / Sponge,Nonresorbable For External UseNAB1Contract manufacturer, Manufactureraccessdata.fda.gov
Lift, Patient, Non-Ac-PoweredFSA1Contract manufacturer, Manufactureraccessdata.fda.gov
Stand, InfusionFOX1Contract manufacturer, Manufactureraccessdata.fda.gov
Stool, Operating-RoomFZM1Contract manufacturer, Manufactureraccessdata.fda.gov
Table, MechanicalINW1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Tips And Pads, Cane, Crutch And WalkerINP1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Tray, Surgical, InstrumentFSM1Contract manufacturer, Manufactureraccessdata.fda.gov
UrinalFNP1Exporter 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
March 14, 2022K213790Aluminum back folding wheelchair SYIV 100-LQXAL2482-407IORSubstantially EquivalentMobility Source Medical Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated March 14, 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.