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Data / Medical devices / Cambodia / Careplus Co., Ltd

Careplus Co., Ltd: FDA-registered device maker in Bavet Svay Rieng, Cambodia, 2 510(k) clearances

Careplus Co., Ltd is registered with the FDA (registration 3031916218) in Bavet Svay Rieng, Cambodia. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 4, 2014. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3031916218
Address
National Road #1, Manhattan SEZ, Sangkat Bavet, Bavet Svay Rieng, Cambodia, 200802
Owner or operator
CAREPLUS CO., LTD (10091235)
Roles
Manufacturer
First device listed
July 29, 2024
Registered through
2026
Brand names listed
ComfortGlide Lateral Transfer Sheet, Hemo-Force SQS/IPCS

Devices it lists

DeviceProduct codeClassRoleSource
Device, Transfer, Patient, ManualFMR1Manufactureraccessdata.fda.gov
Sleeve, Limb, CompressibleJOW2Manufactureraccessdata.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
December 4, 2014K141064VESOFLOW PLUS DVT COMPRESSION DEVICEJOWSubstantially EquivalentCaremed Supply, Inc.accessdata.fda.gov
August 25, 2011K110977VESOFLOWJOWSubstantially EquivalentCaremed Supply, Inc.accessdata.fda.gov

Compare with other makers

Updated December 4, 2014. 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.