Nu Skin Facial Spa

GUDID 00860196000303

NSE PRODUCTS, INC.

Analgesic transcutaneous electrical nerve stimulation system

• Primary Device ID: 00860196000303
• NIH Device Record Key: e4c4ee2d-8b21-4ce2-86cb-6a95f2cb1d8c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nu Skin Facial Spa
• Version Model Number: 90025509
• Company DUNS: 803486393
• Company Name: NSE PRODUCTS, INC.
• Device Count: 1
• DM Exempt: true
• 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: false
• Manufacturing Date: true
• 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: false

Customer Support Contacts

• Phone: +1(801)345-2753
• Email: dtracy@nuskin.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860196000303 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K122711

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: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-10-23
• Device Publish Date: 2016-09-28

Devices Manufactured by NSE PRODUCTS, INC.

• 00850021097554 - Nu Skin RenuSpa iO: 2023-12-05
• 00850021097561 - Nu Skin RenuSpa iO Package: 2023-12-05
• 00850021097578 - AP 24® Smile Pop Toothbrush: 2023-08-21
• 00860196000303 - Nu Skin Facial Spa: 2019-10-23
• 00860196000303 - Nu Skin Facial Spa: 2019-10-23
• 00860196000327 - Nu Skin Facial Spa Package: 2019-10-23
• 00860196000310 - Nu Skin Conductive Gel: 2018-07-06