AviClear

GUDID 00816722022714

Large handpiece for AviClear laser sytsem

CUTERA, INC.

Dermatological solid-state laser system

• Primary Device ID: 00816722022714
• NIH Device Record Key: a93f4238-a18f-48e4-968c-a2ef77487d60
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AviClear
• Version Model Number: AviClear Large handpiece
• 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	00816722022714 [Primary]

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: 2025-08-26
• Device Publish Date: 2025-08-18

On-Brand Devices [AviClear]

• 00816722022707: AviClear Laser Handpiece
• 00816722021700: AviClear Laser System
• 00816722022714: Large handpiece for AviClear laser sytsem