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Data / Medical devices / United States / Heat In A Click LLC

Heat In A Click LLC: FDA-registered device maker in Dania, FL, United States, 6 510(k) clearances

Heat In A Click LLC is registered with the FDA (registration 3008929787) in Dania, FL, United States. It lists 10 device types. The FDA files 6 510(k) clearances under its listings, the newest dated September 26, 2022. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Heat In A Click LLC
FDA registration number
3008929787
Address
1975 Tigertail Blvd, Dania, FL, United States, 33004
Owner or operator
HEAT IN A CLICK LLC (10037785)
Roles
Specification developer
First device listed
September 11, 2016
Registered through
2026
Brand names listed
2Face/ Palm Nrg, Fat Iron, Fit Relief Device, LUMINA NRG, Looper (Model: ZX-579S, Lumina-nrg Fat Iron pro at home body fat slimming & skin tightening device, MINI GLOW, Microcurrent & LED Tightening Sculpting & Wrinkle Reducing Device and more

Devices it lists

DeviceProduct codeClassRoleSource
Brush, Dermabrasion, PoweredGFE1Specification developeraccessdata.fda.gov
Electrosurgical, Cutting & Coagulation & AccessoriesGEI2Specification developeraccessdata.fda.gov
Light Based Over The Counter Wrinkle ReductionOHS2Specification developeraccessdata.fda.gov
Massager, Therapeutic, ElectricISA1Specification developeraccessdata.fda.gov
Massager, Vacuum, Radio Frequency Induced HeatPBX2Specification developeraccessdata.fda.gov
Over-The-Counter Powered Light Based Laser For AcneOLP2Specification developeraccessdata.fda.gov
Static Electricity-Emitting Device, Cosmetic UseNZFNSpecification developeraccessdata.fda.gov
Stimulator, Muscle, Powered, For Muscle ConditioningNGX2Specification developeraccessdata.fda.gov
Stimulator, Nerve, Transcutaneous, Over-The-CounterNUH2Specification developeraccessdata.fda.gov
Stimulator, Transcutaneous Electrical, Aesthetic PurposesNFO2Specification 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
September 26, 2022K214015Palm NRG cellulite body device (model: Palm NRG body device)PBXSubstantially EquivalentHeat IN A Click, LLCaccessdata.fda.gov
July 7, 2022K213056LED Facial MaskOLPSubstantially EquivalentShenzhen Osto Technology Company Limitedaccessdata.fda.gov
April 16, 2021K202055Looper (Model: ZX-579S)OLPSubstantially EquivalentHeat IN A Click, LLCaccessdata.fda.gov
November 3, 2020K191940Palm NRG cellulite and muscle toning body devicePBXSubstantially EquivalentHeat IN A Clickaccessdata.fda.gov
August 28, 2020K191938FitRelief TENS&EMS Wireless DeviceNGXSubstantially EquivalentHeat IN A Click, LLCaccessdata.fda.gov
April 26, 2018K1718212 Face / Face EvolutionNFOSubstantially EquivalentHeat IN A Clickaccessdata.fda.gov

Compare with other makers

Updated September 26, 2022. 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.