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Data / Medical devices / United States / Ideavillage Products Corp.

Ideavillage Products Corp.: FDA-registered device maker in Wayne, NJ, United States, 1 510(k) clearance

Ideavillage Products Corp. is registered with the FDA (registration 2249769) in Wayne, NJ, United States. It lists 17 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 13, 2011. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Ideavillage Products Corp.
FDA registration number
2249769
FEI number
3003185120
Address
155 Route 46 West, 4/F, Wayne, NJ, United States, 07470
Owner or operator
Ideavillage Products Corp. (10031892)
Roles
Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer
First device listed
May 9, 2017
Registered through
2026
Brand names listed
CF Arch Orthotic Insole, CF DUAL ACTION BACK BRACE BELT, CF DUAL ACTION ELBOW GEL, CF ELITE HAMSTRING SLEEVE, CF Easy On-Off Compression Heather Sock, CF Elite Socks, CF HOT-COLD THERAPY 360 FREEZE SLEEVE, CF Insole Plantar Fascitis Orthotic Insole and more

Devices it lists

DeviceProduct codeClassRoleSource
Bandage, ElasticFQM1Complaint file establishment, Specification developeraccessdata.fda.gov
Garment, Protective, For IncontinenceEYQ1Specification developeraccessdata.fda.gov
Insoles, MedicalKYS1Specification developeraccessdata.fda.gov
Joint, Ankle, External BraceITW1Specification developeraccessdata.fda.gov
Joint, Elbow, External Limb Component, MechanicalIRD1Specification developeraccessdata.fda.gov
Joint, Knee, External BraceITQ1Specification developeraccessdata.fda.gov
Joint, Shoulder, External Limb ComponentIQQ1Specification developeraccessdata.fda.gov
Lamp, Infrared, Therapeutic HeatingILY2Specification developeraccessdata.fda.gov
Massager, Therapeutic, ElectricISA1Specification developeraccessdata.fda.gov
Orthosis, LumbarIQE1Specification developeraccessdata.fda.gov
Pack, Hot Or Cold, ReusableIME1Specification developeraccessdata.fda.gov
Splint, Hand, And ComponentsILH1Specification developeraccessdata.fda.gov
Stimulator, Muscle, Powered, For Muscle ConditioningNGX2Repackager or relabeleraccessdata.fda.gov
Stimulator, Nerve, Transcutaneous, Over-The-CounterNUH2Repackager or relabeleraccessdata.fda.gov
Stocking, Medical Support (For General Medical Purposes)FQL1Specification developeraccessdata.fda.gov
Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)DWL2Manufactureraccessdata.fda.gov
Sunglasses (Non-Prescription Including Photosensitive)HQY1Specification developeraccessdata.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 13, 2011K102598HI-DOW-XPNUHSubstantially EquivalentHi-Dow International, Inc.accessdata.fda.gov

Compare with other makers

Updated May 13, 2011. 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.