BEUDAMED
    FDA Registration Active 🇺🇸 United States

    DermLite Lumio S (DLUS)

    Reg #: 3003452144 · FEI: 3003452144 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    36
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    DermLite LLC
    Registration Number
    3003452144
    FEI Number
    3003452144
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    21 Argonaut, Unit A
    City
    Aliso Viejo
    State
    CA
    ZIP
    92656
    Country
    US

    Owner / Operator

    Firm Name
    DermLite LLC
    Operator Number
    9045109
    Address
    21 Argonaut, Unit A
    City
    Aliso Viejo
    State
    CA
    Postal Code
    92656
    Country
    US
    Correspondent
    JOHN - BOTTJER

    Products

    Device Name Product Code
    Light, Examination, Medical, Battery Powered KYT

    Proprietary Names

    DermLite Lumio S (DLUS) DermLite DL100 DermLite 3 (DL3) DermLite II Pro HR (DL2HR) DermLite II Multispectral (DL2MS) DermLite II Pro (DL2Pro) DermLite Pro DP-R DermLite Carbon (DermLite DLC) DermLite Lumio (LUM) DermLite Platinum DermLite 1 (DL1) DermLite Lumio UV (LUM UV) DermLite 1 Basic (DL1B) DermLite 3 (DL3N) SkinLite ALT100-0033 DermLite Cam (DLCAM) Alumina DermLite Foto II Pro (Foto II Pro) DermLite Foto DermLite II Fluid DermLite DL4 (DL4) SkinLite II DermLite II Hybrid (DL2HM) DermLite HUD (HUD-I6) DermLite Foto X DermLite DL200 HYG DermLite DL200 Hybrid Syris v900L DermLite Nailio DermLite DL4W DermLite Lumio 2 (DLU2) DermLite GenLite DermLite DL200 HR DermLite Handyscope DermLite DL5 (DL5) HUD2

    Establishment Types

    Manufacture Medical Device