Angel Aligner

GUDID 06956748709429

Wuxi EA Medical Instruments Technologies Limited.

Orthodontic progressive aligner

• Primary Device ID: 06956748709429
• NIH Device Record Key: c1a8bf95-323e-4f90-a8a8-f9c4ff89a29b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Angel Aligner
• Version Model Number: EAB II
• Company DUNS: 421315681
• Company Name: Wuxi EA Medical Instruments Technologies Limited.
• 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: true
• 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	06956748709429 [Primary]

FDA Product Code

• NXC: Aligner, Sequential

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: 2026-02-12
• Device Publish Date: 2026-02-04

On-Brand Devices [Angel Aligner]

• 06956748701270: EAB II
• 06956748709443: EAB II
• 06956748709436: EAB II
• 06956748709429: EAB II
• 06956748702147: EAB II
• 06956748702062: EAB II
• 06956748702055: EAB II
• 06956748700761: EAB II