BEUDAMED
    FDA Registration Active 🇺🇸 United States

    NOVAPROBE LEUKOS 175

    Reg #: 3010120217 · FEI: 3010120217 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    NOVAPROBE INC.
    Registration Number
    3010120217
    FEI Number
    3010120217
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    17 W 2ND ST, REAR Suite 1001
    City
    Lansdale
    State
    PA
    ZIP
    19446
    Country
    US

    Regulatory Submissions

    510(k) Number
    K131226

    Owner / Operator

    Firm Name
    NovaProbe Inc.
    Operator Number
    10043192
    Address
    207 Warwick Way
    City
    North Wales
    State
    PA
    Postal Code
    19454
    Country
    US
    Correspondent
    Manish Ingle

    Products

    Device Name Product Code
    Laparoscope, General & Plastic Surgery GCJ
    Light Source, Fiberoptic, Routine FCW

    Proprietary Names

    NOVAPROBE LEUKOS 175 NOVAPROBE LED Light source LED LEUKOS 175

    Establishment Types

    Manufacture Medical Device