Progressive

GUDID 06956748701669

Wuxi EA Medical Instruments Technologies Limited.

Orthodontic retainer

• Primary Device ID: 06956748701669
• NIH Device Record Key: cac6bf60-26af-429c-b305-25843c90ff9b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Progressive
• 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06956748701669 [Primary]

FDA Product Code

• DYT: Maintainer, Space Preformed, Orthodontic

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

Devices Manufactured by Wuxi EA Medical Instruments Technologies Limited.

• 06956748700761 - Angel Aligner: 2026-02-12
• 06956748701621 - IMPRESS: 2026-02-12
• 06956748701669 - Progressive: 2026-02-12
• 06956748701669 - Progressive: 2026-02-12
• 06956748701997 - OrthoArch: 2026-02-12
• 06956748702000 - OrthoArch: 2026-02-12
• 06956748702055 - Angel Aligner: 2026-02-12
• 06956748702062 - Angel Aligner: 2026-02-12
• 06956748702147 - Angel Aligner: 2026-02-12