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Data / Medical devices / China / Jiangsu Jumao X-Care Medical Equipment Co., Ltd

Jiangsu Jumao X-Care Medical Equipment Co., Ltd: FDA-registered device maker in Danyang Jiangsu, China, 9 510(k) clearances

Jiangsu Jumao X-Care Medical Equipment Co., Ltd is registered with the FDA (registration 3014810929) in Danyang Jiangsu, China. It lists 37 device types. The FDA files 9 510(k) clearances under its listings, the newest dated May 11, 2026. 1 recall event names it as the recalling firm (1 Class I). Registered through 2026. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this oneWatch Jiangsu Jumao X-Care Medical Equipment Co., Ltd
FDA registration number
3014810929
Address
NO.36 Danyan Road, Danyang Jiangsu, China, 212300
Owner or operator
Jiangsu Jumao X-Care Medical Equipment Co., Ltd (10058053)
Roles
Contract manufacturer, Exporter to the US, Manufacturer
First device listed
June 29, 2018
Registered through
2026
Brand names listed
5-LITER Oxygen Concentrator,A5LC1; JUMAO, 83005, AXLE AND HARDWARE,Seat guides, Anti-tipper, Armrest, Armrest Pad, BACK UPHOLSTERY 19" FOR ATC19, BED, AC-POWERED ADJUSTABLE HOSPITAL and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, WheelchairKNO1Exporter to the US, Manufactureraccessdata.fda.gov
Adaptor, HygieneILS1Manufactureraccessdata.fda.gov
Apparatus, Suction, Ward Use, Portable, Ac-PoweredJCX2Manufactureraccessdata.fda.gov
Armrest, WheelchairIML1Manufactureraccessdata.fda.gov
Attachment, Commode, WheelchairINB1Manufactureraccessdata.fda.gov
Bed, Ac-Powered Adjustable HospitalFNL2Manufactureraccessdata.fda.gov
Bed, ManualFNJ1Manufactureraccessdata.fda.gov
Bed, Patient Rotation, ManualINY1Manufactureraccessdata.fda.gov
Bottle, Collection, VacuumKDQ2Manufactureraccessdata.fda.gov
Brake, Extension, WheelchairIMW1Manufactureraccessdata.fda.gov
Catheter, Nasal, OxygenBZB1Manufactureraccessdata.fda.gov
Chair And Table, MedicalKMN1Contract manufacturer, Manufactureraccessdata.fda.gov
Chair, With CastersINM1Manufactureraccessdata.fda.gov
Components, WheelchairKNN1Manufactureraccessdata.fda.gov
Compressor, Air, PortableBTI2Manufactureraccessdata.fda.gov
CrutchIPR1Manufactureraccessdata.fda.gov
Cushion, WheelchairIMP1Manufactureraccessdata.fda.gov
Cylinder, Compressed Gas, And ValveECX1Manufactureraccessdata.fda.gov
Device, Anti-Tip, WheelchairIMR1Manufactureraccessdata.fda.gov
Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella EuaQKRNManufactureraccessdata.fda.gov
Flowmeter, Calibration, GasBXY1Manufactureraccessdata.fda.gov
Footrest, WheelchairIMM1Manufactureraccessdata.fda.gov
Generator, Oxygen, PortableCAW2Manufactureraccessdata.fda.gov
Humidifier, Non-Direct Patient Interface (Home-Use)KFZ1Manufactureraccessdata.fda.gov
Mask, OxygenBYG1Manufactureraccessdata.fda.gov
Mouthpiece, BreathingBYP1Manufactureraccessdata.fda.gov
Pump, Nebulizer, Electrically PoweredJPW1Manufactureraccessdata.fda.gov
Regulator, Pressure, Gas CylinderCAN1Manufactureraccessdata.fda.gov
Screen, Leaded, Operator Radiation ProtectorEAK1Contract manufacturer, Manufactureraccessdata.fda.gov
Stand, InfusionFOX1Contract manufacturer, Manufactureraccessdata.fda.gov
Table, MechanicalINW1Exporter to the US, Manufactureraccessdata.fda.gov
Tray, Surgical, InstrumentFSM1Contract manufacturer, Manufactureraccessdata.fda.gov
Tube, Aspirating, Flexible, ConnectingBYY2Manufactureraccessdata.fda.gov
Unit, Filter, MembraneJRL1Exporter to the US, Manufactureraccessdata.fda.gov
Walker, MechanicalITJ1Manufactureraccessdata.fda.gov
Wheelchair, MechanicalIOR1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Wheelchair, PoweredITI2Manufactureraccessdata.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
May 11, 2026K250964Protable Phlegm Suction Unit (JMA D01)JCXSubstantially EquivalentJiangsu Jumao X-Care Medical Equipment Co., Ltd.accessdata.fda.gov
January 29, 2026K253632Manual Wheelchair (W50)IORSubstantially EquivalentJiangsu Jumao X-Care Medical Equipment Co., , Ltd.accessdata.fda.gov
December 5, 2025K252828Manual Wheelchair (W47)IORSubstantially EquivalentJiangsu Jumao X-Care Medical Equipment Co., , Ltd.accessdata.fda.gov
December 5, 2025K252825Manual Wheelchair (W45)IORSubstantially EquivalentJiangsu Jumao X-Care Medical Equipment Co., , Ltd.accessdata.fda.gov
August 21, 2025K251130Portable Oxygen Concentrator (JM-P50A)CAWSubstantially EquivalentJiangsu Jumao X-Care Medical Equipment Co., Ltd.accessdata.fda.gov
January 19, 2024K232783Power wheelchair (Model: JMPW-01W)ITISubstantially EquivalentJiangsu Jumao X-Care Medical Equipment Co., Ltd.accessdata.fda.gov
November 9, 2023K230969Oxygen ConcentratorCAWSubstantially EquivalentJiangsu Jumao X-Care Medical Equipment Co., Ltd.accessdata.fda.gov
June 14, 2021K200466Manual Wheelchair (Model W28)IORSubstantially EquivalentJiangsu Jumao X-Care Medical Equipment Co., Ltd.accessdata.fda.gov
July 24, 2009K090007JUMAO OXYGEN CONCENTRATOR, MODEL JM-07000HI, JM-07000I, JM-07000CAWSubstantially EquivalentDanyang Jumao Healthcare Equipment Co., Ltd.accessdata.fda.gov

Recalls

Recall events where this establishment is the recalling firm, matched on its FEI.

InitiatedEventClassStatusProductReasonSource
December 9, 202495818Class IOngoingJMC5A Ni/TruAire-5 Oxygen Concentrator, Model: O2C5LOxygen concentrator may melt or catch on fire during use.accessdata.fda.gov

Compare with other makers

Updated May 11, 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.