BEUDAMED
    FDA Registration Active 🇺🇸 United States

    EpiCare Alexandrite Laser, Model 501-LP

    Reg #: 3015730775 · FEI: 3015730775 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    LASETECH, LLC
    Registration Number
    3015730775
    FEI Number
    3015730775
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    11 Princess Road, Ste C
    City
    Lawrenceville
    State
    NJ
    ZIP
    08648
    Country
    US

    Regulatory Submissions

    510(k) Number
    K032991

    Owner / Operator

    Firm Name
    LaseTech LLC
    Operator Number
    10092722
    Address
    11 Princess Road, Ste C
    City
    Lawrenceville
    State
    NJ
    Postal Code
    08648
    Country
    US
    Correspondent
    Bruce Wade

    Products

    Device Name Product Code
    Powered Laser Surgical Instrument GEX

    Proprietary Names

    EpiCare Alexandrite Laser, Model 501-LP EpiCare Alexandrite Laser, Model 501-LPX EpiCare Zenith Alexandrite Laser, Model 504-ZTHA

    Establishment Types

    Manufacture Medical Device