Reveal® Aligners

GUDID 00190707096922

Reveal® Aligners FLEX

Ortho Organizers, Inc.

Orthodontic progressive aligner

• Primary Device ID: 00190707096922
• NIH Device Record Key: 12d3c9b3-de15-445d-92cd-93eae373d932
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reveal® Aligners
• Version Model Number: 139-6325
• Company DUNS: 062165188
• Company Name: Ortho Organizers, 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00190707096922 [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: 2025-12-19
• Device Publish Date: 2022-01-06

On-Brand Devices [Reveal® Aligners]

• 00190707096922: Reveal® Aligners FLEX
• 00190707096915: Reveal® Aligners STANDARD
• 00190707096908: Reveal® Aligners Remake
• 00190707096892: Reveal® Aligners
• 00190707096885: Reveal® Aligners
• 00190707096878: Reveal® Aligners
• 00190707096861: Reveal® Aligners
• 00190707096854: Reveal® Aligners
• 00190707096847: Reveal® Aligners
• 00190707096830: Reveal® Aligners
• 00190707096823: Reveal® Aligners
• 00190707096816: Reveal® Aligners
• 00190707096809: Reveal® Aligners
• 00190707096793: Reveal® Aligners
• 00190707096786: Reveal® Aligners
• 00190707096779: Reveal® Aligners
• 00190707096762: Reveal® Aligners
• 00190707096755: Reveal® Aligners