BEUDAMED
    FDA Registration Active 🇺🇸 United States

    AcuTip 500, Limelight, ProWave 770, ProWave LX

    Reg #: 2954354 · FEI: 3002900199 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    CUTERA, INC.
    Registration Number
    2954354
    FEI Number
    3002900199
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    3240 BAYSHORE BLVD
    City
    BRISBANE
    State
    CA
    ZIP
    94005
    Country
    US

    Regulatory Submissions

    510(k) Number
    K050047

    Owner / Operator

    Firm Name
    Cutera, Inc.
    Operator Number
    9038697
    Address
    3240 Bayshore Blvd.
    City
    Brisbane
    State
    CA
    Postal Code
    94005
    Country
    US

    Products

    Device Name Product Code
    Powered Laser Surgical Instrument GEX

    Proprietary Names

    AcuTip 500, Limelight, ProWave 770, ProWave LX

    Establishment Types

    Manufacture Medical Device