sensiLift

GUDID 05060445341125

The sensiLift is an over-the-counter home use device intended for non-invasive treatment of mild to moderate facial wrinkles for adult women who have Fitzpatrick Skin Types I-IV.

EL GLOBAL TRADE LTD

Radio-frequency skin surface treatment system

• Primary Device ID: 05060445341125
• NIH Device Record Key: 3bfff1f2-3075-42d6-bca3-8c99adfd9d19
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: sensiLift
• Version Model Number: ST100US01SNS
• Company DUNS: 649726981
• Company Name: EL GLOBAL TRADE LTD
• 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: false
• 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: 855-736-7422
• Email: support@sensica.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060445341125 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170499

FDA Product Code

• PAY: Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-07
• Device Publish Date: 2017-08-16

On-Brand Devices [sensiLift]

• 05060445341255: The Sensilift is an over-the-counter home use device intended for non-invasive treatment of mild
• 05060445341125: The sensiLift is an over-the-counter home use device intended for non-invasive treatment of mild