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Data / Medical devices / China / Jan Mao Industries Co., Ltd.

Jan Mao Industries Co., Ltd.: FDA-registered device maker in Guangxi Zhuang Autonomous Region, China, 3 510(k) clearances

Jan Mao Industries Co., Ltd. is registered with the FDA (registration 3009596133) in Guangxi Zhuang Autonomous Region, China. It lists 29 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 16, 2006. Registered through 2027. FDA data exported November 2, 2026.

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Get makers like this oneWatch Jan Mao Industries Co., Ltd.
FDA registration number
3009596133
Address
No. 15, Yuanqu Avenue, Xin an Town, Pingguo City Baise City, Guangxi Zhuang Autonomous Region, China, 531400
Owner or operator
Jan Mao Industries Co., Ltd. (9008785)
Roles
Exporter to the US, Manufacturer
First device listed
January 5, 1994
Registered through
2027
Brand names listed
ADJUSTABLE, CANE, CANE AND CRUTCH TIPS AND PADS, CRUTCH, Chair, Geriatric, Chair,With Casters, Daily activity assist device, Emergency Cart and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, WheelchairKNO1Exporter to the US, Manufactureraccessdata.fda.gov
Accessory, Surgical ApparelLYU1Exporter to the US, Manufactureraccessdata.fda.gov
Adaptor, HygieneILS1Exporter to the US, Manufactureraccessdata.fda.gov
Adaptor, RecreationalILT1Exporter to the US, Manufactureraccessdata.fda.gov
Aid, TransferIKX1Exporter to the US, Manufactureraccessdata.fda.gov
Apparatus, Traction, Non-PoweredHST1Exporter to the US, Manufactureraccessdata.fda.gov
Attachment, Commode, WheelchairINB1Exporter to the US, Manufactureraccessdata.fda.gov
Bed, ManualFNJ1Exporter to the US, Manufactureraccessdata.fda.gov
Bottle, Collection, VacuumKDQ2Exporter to the US, Manufactureraccessdata.fda.gov
CaneIPS1Exporter to the US, Manufactureraccessdata.fda.gov
Cap, SurgicalFYF1Exporter to the US, Manufactureraccessdata.fda.gov
Cart, Emergency, Cardiopulmonary (Excluding Equipment)BZN1Exporter to the US, Manufactureraccessdata.fda.gov
Chair, GeriatricFRJ1Exporter to the US, Manufactureraccessdata.fda.gov
Chair, With CastersINM1Exporter to the US, Manufactureraccessdata.fda.gov
Components, WheelchairKNN1Exporter to the US, Manufactureraccessdata.fda.gov
Cover, Shoe, Operating-RoomFXP1Exporter to the US, Manufactureraccessdata.fda.gov
CrutchIPR1Exporter to the US, Manufactureraccessdata.fda.gov
Delivery Room Apparel KitPWV1Exporter to the US, Manufactureraccessdata.fda.gov
Dispenser, Liquid MedicationKYX1Exporter to the US, Manufactureraccessdata.fda.gov
Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella EuaQKRNExporter to the US, Manufactureraccessdata.fda.gov
Non-Surgical GownOEA1Exporter to the US, Manufactureraccessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)HOY1Exporter to the US, Manufactureraccessdata.fda.gov
Stand, InfusionFOX1Exporter to the US, Manufactureraccessdata.fda.gov
Support, Breathing TubeJAY1Exporter to the US, Manufactureraccessdata.fda.gov
Table, MechanicalINW1Exporter to the US, Manufactureraccessdata.fda.gov
Tips And Pads, Cane, Crutch And WalkerINP1Exporter to the US, Manufactureraccessdata.fda.gov
Tray, Surgical, InstrumentFSM1Exporter 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
August 16, 2006K062218JAN MAO WHEELCHAIR, MODELS JMC612-FL318EPP AND JMC612-FL418EPPIORSubstantially EquivalentJan Mao Industries Co., Ltd.accessdata.fda.gov
June 29, 2005K051482JAN MAO WHEELCHAIR, MODEL JMC612-F18EPPIORSubstantially EquivalentJan Mao Industries Co., Ltd.accessdata.fda.gov
June 29, 2005K051481JAN MAO WHEELCHAIR, MODEL JMC611-F18EPPIORSubstantially EquivalentJan Mao Industries Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated August 16, 2006. 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.