Xpect Vision

GUDID 06978898058042

Shenzhen Cresendo Technology Co.,Ltd.

Air-conduction hearing aid, in-the-ear

• Primary Device ID: 06978898058042
• NIH Device Record Key: 4aa6ca4d-fcba-402d-99d0-8ed1d1cf5596
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Xpect Vision
• Version Model Number: XVG
• Company DUNS: 509812622
• Company Name: Shenzhen Cresendo Technology Co.,Ltd.
• 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: false
• Serial Number: true
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06978898058042 [Primary]

FDA Product Code

• QUF: Hearing Aid, Air-Conduction, Over The Counter

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: 2025-12-22
• Device Publish Date: 2025-12-12

On-Brand Devices [Xpect Vision]

• 06978898058066: XVC
• 06978898058059: XVH
• 06978898058042: XVG