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Data / Medical devices / United States / Conair LLC.

Conair LLC.: FDA-registered device maker in Stamford, CT, United States, 5 510(k) clearances

Conair LLC. is registered with the FDA (registration 1222304) in Stamford, CT, United States. It lists 11 device types. The FDA files 5 510(k) clearances under its listings, the newest dated March 14, 2019. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1222304
FEI number
1000121041
Address
1 Cummings Point RD., Stamford, CT, United States, 06902
Owner or operator
Conair LLC. (2242745)
Roles
Complaint file establishment, Specification developer
First device listed
May 7, 1991
Registered through
2026
Brand names listed
AC POWERED AND BATTERY POWERED, CONAIR, CONAIR HEATING PAD, CONAIR INTERPAK WATER TEST, Conair, Conair Infrared Thermometer, Interplank, Lumilisse and more

Devices it lists

DeviceProduct codeClassRoleSource
Analyzer, Body CompositionMNW2Complaint file establishmentaccessdata.fda.gov
Bath, ParaffinIMC2Complaint file establishment, Specification developeraccessdata.fda.gov
Continuous Measurement ThermometerFLL2Complaint file establishmentaccessdata.fda.gov
Light Based Over The Counter Wrinkle ReductionOHS2Complaint file establishmentaccessdata.fda.gov
Light Based Over-The-Counter Hair RemovalOHT2Complaint file establishmentaccessdata.fda.gov
Massager, Therapeutic, ElectricISA1Complaint file establishment, Specification developeraccessdata.fda.gov
Over-The-Counter Powered Light Based Laser For AcneOLP2Complaint file establishmentaccessdata.fda.gov
Pad, Heating, PoweredIRT2Complaint file establishment, Specification developeraccessdata.fda.gov
Powered Light Based Non-Laser Surgical Instrument With Thermal EffectONF2Complaint file establishmentaccessdata.fda.gov
Toothbrush, PoweredJEQ1Complaint file establishment, Specification developeraccessdata.fda.gov
Unit, Oral IrrigationEFS1Complaint file establishment, Specification 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
March 14, 2019K183247dpl FacewareOHSSubstantially EquivalentLed Technologies, Inc.accessdata.fda.gov
January 18, 2018K172791Lumilisse IPL Hair RemoverOHTSubstantially EquivalentConair Corporationaccessdata.fda.gov
March 31, 2015K141181NUVE FOR WRINKLES, DPL NUVE FOR WRINKLESOHSSubstantially EquivalentLed Technologies, LLCaccessdata.fda.gov
August 21, 2014K140681BELTER INFRA-RED EAR THERMOMETERFLLSubstantially EquivalentShenzhen Belter Health Measurement and Analysis TEaccessdata.fda.gov
October 5, 2001K010706THINNER RESOLVE FITNESS MONITOR/BODY SCALE, HEALTH-O-METERMNWSubstantially EquivalentMeasurement Specialties, Inc.accessdata.fda.gov

Compare with other makers

Updated March 14, 2019. 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.