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    LTS Therapy Systems, LLC

    FDA registration
    LTS Therapy Systems, LLC·1 product·🇺🇸 United States

    Travanti

    FDA UDI
    LTS Therapy Systems, LLC·20815611021009·This kit contains two (2) devices: 1) IontoPa...

    IontoPatch

    FDA UDI
    LTS Therapy Systems, LLC·10815611020012·The IontoPatch contains an innovative self-cont...

    IontoPatch

    FDA UDI
    LTS Therapy Systems, LLC·10815611020036·The IontoPatch contains an innovative self-cont...

    Travanti

    FDA UDI
    LTS Therapy Systems, LLC·20815611021030·This kit contains two (2) devices: 1) IontoPa...

    IontoPatch

    FDA UDI
    LTS Therapy Systems, LLC·10815611020029·The IontoPatch contains an innovative self-cont...

    Travanti

    FDA UDI
    LTS Therapy Systems, LLC·20815611021016·This kit contains two (2) devices: 1) IontoPa...

    IontoPatch

    FDA UDI
    LTS Therapy Systems, LLC·10815611020005·The IontoPatch contains an innovative self-cont...

    Travanti

    FDA UDI
    LTS Therapy Systems, LLC·20815611021023·This kit contains two (2) devices: 1) IontoPa...

    IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch.

    FDA Recall
    Open, Classified ·LTS Therapy Systems, LLC·Product code EGJ·May 22, 2025

    IontoPatch 80, On-the-Go Patch Therapy, Model/Catalog Number: D-0077-080; The IontoPatch is an Iontophoresis transdermal patch.

    FDA Recall
    Open, Classified ·LTS Therapy Systems, LLC·Product code EGJ·May 22, 2025

    IontoPatch 80, On-the-Go Patch Therapy, Model/Catalog Number: D-0077-080; The IontoPatch is an Iontophoresis transdermal patch.

    FDA Enforcement
    Class II ·Ongoing·LTS Therapy Systems, LLC·August 6, 2025

    IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch.

    FDA Enforcement
    Class II ·Ongoing·LTS Therapy Systems, LLC·August 6, 2025

    The Ebb Complete Tamponade System, model #CTS-1000 and Code #OQY. Intended for use in providing temporary control or reduction of postpartum uterine bleeding.

    FDA Enforcement
    Class II ·Terminated·Clinical Innovations, LLC·October 21, 2015