BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Magic Science Supply LLC

    Reg #: 3010610560 · FEI: 3010610560 · Expires 2026
    View on FDA
    Products
    1
    Proprietary Names
    20
    Establishment Types
    5
    Classifications
    1

    Registration Details

    Registration Name
    Magic Science Supply LLC
    Registration Number
    3010610560
    FEI Number
    3010610560
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    5555 W 78th St Ste M
    City
    Edina
    State
    MN
    ZIP
    55439
    Country
    US

    Regulatory Submissions

    510(k) Number
    K160095

    Owner / Operator

    Firm Name
    Magic Science Supply LLC
    Operator Number
    10053463
    Address
    5555 W 78th St, STE D & M
    City
    Edina
    State
    MN
    Postal Code
    55439
    Country
    US
    Correspondent
    Patrick Harasyn

    Products

    Device Name Product Code
    Dressing, Wound, Drug FRO

    Proprietary Names

    SkinSmart Antimicrobial Foot Cleanser SkinSmart Antimicrobial Perineal Cleanser SkinSmart Antimicrobial Skin and Wound Cleanser (Piercing and Tattoo Aftercare) SkinSmart Antimicrobial Facial Cleanser (Acne) Magic Molecule Antimicrobial Skin Cleanser Magic Molecule Antimicrobial Skin Spray SkinSmart Antimicrobial Eczema Therapy CleanSmart Antimicrobial Hand Cleanser SkinSmart Antimicrobial Men's Skin Cleanser (Intimate Body Spray) SkinSmart Antimicrobial Skin Cleanser (Nipple Spray) Magic Molecule Antimicrobial Skin Spray for Pets SkinSmart Antimicrobial Skin Cleanser (Eczema Spray for Babies and Toddlers) SkinSmart Antimicrobial First Aid Skin Wash (Rash and Hive Care) SkinSmart Antimicrobial Skin Cleanser for Pets SkinSmart Antimicrobial Facial Cleanser (Virus) SkinSmart Antimicrobial Skin Cleanser for Pets (Hot Spot Spray) SkinSmart Antimicrobial Wound Therapy CleanSmart Skin and Wound Cleanser DermaSmart Skin Cleanser (Eczema) Simple Science Antimicrobial Facial and Eyelid Cleanser

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Remanufacture Medical Device Manufacture Medical Device