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Data / Medical devices / United States / Pain Management Technologies

Pain Management Technologies: FDA-registered device maker in Akron, OH, United States, 26 510(k) clearances

Pain Management Technologies is registered with the FDA (registration 1528161) in Akron, OH, United States. It lists 21 device types. The FDA files 26 510(k) clearances under its listings, the newest dated November 27, 2024. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
1528161
FEI number
1000122747
Address
1760 Wadsworth Rd, Akron, OH, United States, 44320
Owner or operator
PAIN MANAGEMENT TECHNOLOGIES (9002150)
Roles
Complaint file establishment
First device listed
July 27, 2005
Registered through
2027
Brand names listed
Aqua Relief System (AIS/ARS), Blue Silver Body Wrap, Blue Silver Cervical, Blue Silver Electric Knee, Brightwand, Brightwand Cordless, CR2000, DIGIGAL and more

Devices it lists

DeviceProduct codeClassRoleSource
Electrode, CutaneousGXY2Complaint file establishmentaccessdata.fda.gov
Interferential Current TherapyLIH2Complaint file establishmentaccessdata.fda.gov
Joint, Knee, External BraceITQ1Complaint file establishmentaccessdata.fda.gov
Lamp, Infrared, Therapeutic HeatingILY2Complaint file establishmentaccessdata.fda.gov
Light, Ultraviolet, DermatologicalFTC2Complaint file establishmentaccessdata.fda.gov
Massager, Therapeutic, ElectricISA1Complaint file establishmentaccessdata.fda.gov
Media, ElectroconductiveGYB2Complaint file establishmentaccessdata.fda.gov
Orthosis, CervicalIQK1Complaint file establishmentaccessdata.fda.gov
Orthosis, LumbarIQE1Complaint file establishmentaccessdata.fda.gov
Pack, Hot Or Cold, ReusableIME1Complaint file establishmentaccessdata.fda.gov
Pack, Hot Or Cold, Water CirculatingILO2Complaint file establishmentaccessdata.fda.gov
Pad, Heating, PoweredIRT2Complaint file establishmentaccessdata.fda.gov
Stationary Ultrasonic Diathermy Device For Use In Applying Therapeutic Deep HeatPFW2Complaint file establishmentaccessdata.fda.gov
Stimulator, Electrical, Non-Implantable, For IncontinenceKPI2Complaint file establishmentaccessdata.fda.gov
Stimulator, Electrical, Transcutaneous, For ArthritisNYN2Complaint file establishmentaccessdata.fda.gov
Stimulator, Muscle, PoweredIPF2Complaint file establishmentaccessdata.fda.gov
Stimulator, Muscle, Powered, For Muscle ConditioningNGX2Complaint file establishmentaccessdata.fda.gov
Stimulator, Nerve, Transcutaneous, For Pain ReliefGZJ2Complaint file establishmentaccessdata.fda.gov
Stimulator, Nerve, Transcutaneous, Over-The-CounterNUH2Complaint file establishmentaccessdata.fda.gov
Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep HeatIMG2Complaint file establishmentaccessdata.fda.gov
Vehicle, Motorized 3-WheeledINI2Complaint file establishmentaccessdata.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
November 27, 2024K241899Pelvic Floor Stimulator (Intrelief PFE)KPISubstantially EquivalentEasymed Instruments Co., Ltd.accessdata.fda.gov
July 19, 2024K233067Wireless TENS & EMS (Model SM9110,SM9113,SM9116)NUHSubstantially EquivalentChongqing Rob Linka Science and Technology Co., Ltd.accessdata.fda.gov
December 13, 2022K222770Conductive GelGYBSubstantially EquivalentTop-Rank Health Care Co., Ltd.accessdata.fda.gov
December 30, 2021K211263IntreliefNUHSubstantially EquivalentEasymed Instruments Co., Ltd.accessdata.fda.gov
June 25, 2021K201196Scooter (Model: FDB01)INISubstantially EquivalentNanjing Jin Bai HE Medical Apparatus Co., Ltd.accessdata.fda.gov
December 19, 2019K192589Everyway OTC TENS/EMS CombinationNUHSubstantially EquivalentEveryway Medical Instruments Co.,Ltdaccessdata.fda.gov
May 29, 2015K143430SmartTENSNUHSubstantially EquivalentEasy Med Instrument Co., Ltd.accessdata.fda.gov
November 17, 2014K142099CUTANEOUS ELECTRODESGXYSubstantially EquivalentBio Protech, Inc.accessdata.fda.gov
September 3, 2014K140865INFRARED HEATING DEVICEILYSubstantially EquivalentPro Medical Supplies, Inc.accessdata.fda.gov
August 28, 2014K140168EASYSTIM TN28_OTCNUHSubstantially EquivalentEasymed Instruments Co., Ltd.accessdata.fda.gov
January 30, 2014K132643UV PHOTOTHERAPYFTCSubstantially EquivalentXuzhou Kernel Medical Equipment Co., Ltd.accessdata.fda.gov
November 22, 2013K132588ADHESIVE ELECTRODESGXYSubstantially EquivalentTop-Rank Health Care Equipment Co., Ltd.accessdata.fda.gov
August 24, 2011K103719LIFECARE CONDUCTIVE GARMENTSGXYSubstantially EquivalentEveryway Medical Instruments Co.,Ltdaccessdata.fda.gov
June 20, 2011K110509EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908LIHSubstantially EquivalentEveryway Medical Instruments Co.,Ltdaccessdata.fda.gov
February 12, 2010K093138MT9000 SERIES ELECTRO-STIMULATOR, MODELS MT9000, MT9002, MT9001, MT9004 AND MT9003IPFSubstantially EquivalentShenzhen Dongdixin Technology Co., Ltd.accessdata.fda.gov
January 14, 2010K092627CT2011 SONICSTIMU PAIN RELIEF DEVICEIMGSubstantially EquivalentShenzhen Dongdixin Technology Co., Ltd.accessdata.fda.gov
January 6, 2009K083494ULTIMA FIVEGZJSubstantially EquivalentPain Management Technologiesaccessdata.fda.gov
July 30, 2008K073386JOINT STIM, MODEL 1000NYNSubstantially EquivalentPain Management Technologiesaccessdata.fda.gov
March 12, 2008K072256HF54 COMBINATION ULTRASOUND INTERFERENTIAL AND PREMODULATED STIMULATION SYSTEM WITH OPTIONAL HANDS-FREE OPERATION, MODELPFWSubstantially EquivalentHill Laboratories Co.accessdata.fda.gov
December 12, 2005K050921EASYSTIM NMS-28IPFSubstantially EquivalentEasy Med Instrument Co., Ltd.accessdata.fda.gov
September 3, 2004K042301PROTENS ELECTRODEGXYSubstantially EquivalentBio Protech, Inc.accessdata.fda.gov
April 8, 2004K040253EASY MED TN-28 CGZJSubstantially EquivalentEasy Med Instrument Co., Ltd.accessdata.fda.gov
December 16, 2003K032994GM3 SERIES HV TENS, MODEL GM3X3HV (WHERE X IS PARAMETER OF DIFFERENT HOUSING)GZJSubstantially EquivalentGemore Technology Co, Ltd.accessdata.fda.gov
May 5, 2003K030375SOFT-TOUCH TENS ELECTRODEGXYSubstantially EquivalentPain Management Technologiesaccessdata.fda.gov
December 20, 2002K024036PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000IPFSubstantially EquivalentJohari Digital Healthcare , Ltd.accessdata.fda.gov
February 5, 2002K012463LIFECARE 5*5 CM SQUARE, LIFECARE 4*4 CM SQUARE, LIFECARE 5 CM ROUND, LIFECARE 7.5 CM ROUND, LIFECARE 4*6 CM OVALGXYSubstantially EquivalentEveryway Medical Instruments Co.,Ltdaccessdata.fda.gov

Compare with other makers

Updated November 27, 2024. 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.