Realine

GUDID 00816063020097

Aligner

ALIGN TECHNOLOGY, INC.

Orthodontic appliance system, progressive

• Primary Device ID: 00816063020097
• NIH Device Record Key: 4ba8925e-c847-476c-9dd9-04034affa913
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Realine
• Version Model Number: 8554
• Company DUNS: 013831768
• Company Name: ALIGN TECHNOLOGY, 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: false
• 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	00816063020097 [Primary]

FDA Product Code

• NXC: Aligner, Sequential

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

Devices Manufactured by ALIGN TECHNOLOGY, INC.

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• 00816063022237 - iTero Lumina Pro Mobile: 2024-11-27 iTero Lumina Pro US Mobile Configuration
• 00816063022268 - iTero Lumina Pro intraoral scanning unit: 2024-11-27 iTero Lumina Pro Scanning Unit, RMA Package US