Trophy Skin

GUDID 00851561006105

RejuvatoneMD Facial Toning Device

TROPHY SKIN, INC

Hand-held deep-tissue electromagnetic stimulator

• Primary Device ID: 00851561006105
• NIH Device Record Key: b0f50c58-ec18-41f5-a8d4-a98d9f3a2ab7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trophy Skin
• Version Model Number: REJUVATONEMD
• Company DUNS: 014294023
• Company Name: TROPHY SKIN, INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 866-546-4664
• Email: sales@trophyskin.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851561006105 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K152199

FDA Product Code

• NFO: Stimulator, Transcutaneous Electrical, Aesthetic Purposes

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-02-10
• Device Publish Date: 2020-01-31

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• 00851561006105: RejuvatoneMD Facial Toning Device