BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Tripollar Device

    Reg #: 3020659203 · FEI: 3020659203 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Passiflora inc.
    Registration Number
    3020659203
    FEI Number
    3020659203
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    Passiflora Inc., 1000 5th Street Suite 200
    City
    Miami Beach
    State
    FL
    ZIP
    33139
    Country
    US

    Regulatory Submissions

    510(k) Number
    K203665

    Owner / Operator

    Firm Name
    Passiflora Inc
    Operator Number
    10061598
    Address
    Passiflora Inc., 1000 5th Street Suite 200
    City
    Miami Beach
    State
    FL
    Postal Code
    33139
    Country
    US
    Correspondent
    Moran S Tabak

    Products

    Device Name Product Code
    Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction PAY

    Proprietary Names

    Tripollar Device

    Establishment Types

    Repack or Relabel Medical Device