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Data / Medical devices / Taiwan / Care&Care Health Products Co., Ltd

Care&Care Health Products Co., Ltd: FDA-registered device maker in Yuanli Township Miaoli, Taiwan, 1 510(k) clearance

Care&Care Health Products Co., Ltd is registered with the FDA (registration 3008351005) in Yuanli Township Miaoli, Taiwan. It lists 32 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 18, 2012. Registered through 2027. FDA data exported November 2, 2026.

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Get makers like this oneWatch Care&Care Health Products Co., Ltd
FDA registration number
3008351005
Address
No. 198, Daxing Rd., Yuanli Township Miaoli, Taiwan, 358006
Owner or operator
Care&Care Health Products Co., Ltd (10032051)
Roles
Exporter to the US, Manufacturer
First device listed
April 5, 2010
Registered through
2027
Brand names listed
AC-Powered Patient Lift, Airemed, Bedpan, Blood Pressure Measurement, Cane, Caster with Chair, Crutch and Cane Holder, Head and Trunk Support and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, WheelchairKNO1Exporter to the US, Manufactureraccessdata.fda.gov
Adaptor, HygieneILS1Exporter to the US, Manufactureraccessdata.fda.gov
Aid, TransferIKX1Exporter to the US, Manufactureraccessdata.fda.gov
Armboard, WheelchairIMY1Exporter to the US, Manufactureraccessdata.fda.gov
Armrest, WheelchairIML1Exporter to the US, Manufactureraccessdata.fda.gov
BedpanFOB1Exporter to the US, Manufactureraccessdata.fda.gov
Belt, WheelchairIQB1Exporter to the US, Manufactureraccessdata.fda.gov
Board, Lap, WheelchairIMX1Exporter to the US, Manufactureraccessdata.fda.gov
Board, Scooter, ProneKNL1Exporter to the US, Manufactureraccessdata.fda.gov
Brake, Extension, WheelchairIMW1Exporter to the US, Manufactureraccessdata.fda.gov
CaneIPS1Exporter to the US, Manufactureraccessdata.fda.gov
Chair, Adjustable, MechanicalINN1Exporter to the US, Manufactureraccessdata.fda.gov
Chair, With CastersINM1Exporter to the US, Manufactureraccessdata.fda.gov
Climber, Curb, WheelchairIMN1Exporter to the US, Manufactureraccessdata.fda.gov
Components, WheelchairKNN1Exporter to the US, Manufactureraccessdata.fda.gov
Cuff, Pusher, WheelchairINC1Exporter to the US, Manufactureraccessdata.fda.gov
Cushion, WheelchairIMP1Exporter to the US, Manufactureraccessdata.fda.gov
Device, Anti-Tip, WheelchairIMR1Exporter to the US, Manufactureraccessdata.fda.gov
Device, Transfer, Patient, ManualFMR1Exporter to the US, Manufactureraccessdata.fda.gov
Exerciser, Non-MeasuringION1Exporter to the US, Manufactureraccessdata.fda.gov
Exerciser, PoweredBXB1Exporter to the US, Manufactureraccessdata.fda.gov
Handrim, WheelchairIMO1Exporter to the US, Manufactureraccessdata.fda.gov
Hill Holder, WheelchairINA1Exporter to the US, Manufactureraccessdata.fda.gov
Holder, Crutch And Cane, WheelchairIMZ1Exporter to the US, Manufactureraccessdata.fda.gov
Lift, Patient, Ac-PoweredFNG2Exporter to the US, Manufactureraccessdata.fda.gov
Mattress, Air Flotation, Alternating PressureFNM2Exporter to the US, Manufactureraccessdata.fda.gov
Restraint, Wheelchair, Non-ProtectiveKID1Exporter to the US, Manufactureraccessdata.fda.gov
Stand, InfusionFOX1Exporter to the US, Manufactureraccessdata.fda.gov
Support, Head And Trunk, WheelchairIMS1Exporter to the US, Manufactureraccessdata.fda.gov
System, Measurement, Blood-Pressure, Non-InvasiveDXN2Exporter to the US, Manufactureraccessdata.fda.gov
Table, MechanicalINW1Exporter to the US, Manufactureraccessdata.fda.gov
Walker, MechanicalITJ1Exporter 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
January 18, 2012K112825AVITA ARM TYPE BLOOD PRESSURE MONITORDXNSubstantially EquivalentAvita Corporationaccessdata.fda.gov

Compare with other makers

Updated January 18, 2012. 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.