FDA Registration Active 🇺🇸 United States

SkinSmart Antimicrobial Facial Cleanser (Acne)

Reg #: 3010610560 · FEI: 3010610560 · Expires 2025
Products
1
Proprietary Names
25
Establishment Types
5
Classifications
1

Registration Details

Registration Name
Magic Science Supply LLC
Registration Number
3010610560
FEI Number
3010610560
Status
Active
Expiry Year
2025
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 Facial Cleanser (Acne) SkinSmart Antimicrobial Skin and Wound Cleanser (Piercing and Tattoo Aftercare) SkinSmart Antimicrobial Perineal Cleanser SkinSmart Antimicrobial Men's Intimate Care SkinSmart Antimicrobial First Aid Skin Wash (Rash) Chapter Twenty Antimicrobial Skin Cleanser SkinSmart Antimicrobial Foot Cleanser SkinSmart Antimicrobial Skin Cleanser for Eczema Therapy SkinSmart Antimicrobial Skin Cleanser for Pets SkinSmart Antimicrobial Piercing and Tattoo Aftercare SkinSmart Antimicrobial Men's Skin Cleanser (Intimate Body Spray) SkinSmart Antimicrobial Rash and Hive Care SkinSmart Antimicrobial Face Cleanser (Virus) SkinSmart Antimicrobial Wound and Skin Cleanser for Wound Therapy CleanSmart Antimicrobial Skin Cleanser NovaGran Antimicrobial Wound Solution Magic Molecule Antimicrobial Skin Cleanser SkinSmart Antimicrobial First Aid Skin Wash (Rash and Hive Care) SkinSmart Antimicrobial Skin Cleanser (Eczema Therapy) SkinSmart Antimicrobial Skin Cleanser (Baby Eczema) SkinSmart Antimicrobial Skin Cleanser for Pets (Hot Spot Spray) SkinSmart Antimicrobial Skin Cleanser (Nipple Spray) SkinSmart Antimicrobial Face Cleanser (Acne) SkinSmart Antimicrobial Facial Cleanser (Virus) Magic Molecule Antimicrobial Skin Spray

Establishment Types

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