AviClear

GUDID 00816722022707

AviClear Laser Handpiece

CUTERA, INC.

Dermatological solid-state laser system

• Primary Device ID: 00816722022707
• NIH Device Record Key: a78bb2ae-5fc0-448f-b98e-cd0fd18187de
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AviClear
• Version Model Number: AviClear
• Company DUNS: 041071643
• Company Name: CUTERA, 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: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816722022707 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K213461

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2022-04-11
• Device Publish Date: 2022-04-01

On-Brand Devices [AviClear]

• 00816722022707: AviClear Laser Handpiece
• 00816722021700: AviClear Laser System