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CEARVOL Wave

by Shenzhen Cannice Technology Co., Ltd 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06980305290075 UDI-DI Date15 Jul 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Cearvol
Generic Name
Air-conduction hearing aid, in-the-ear
Model / Reference
Wave
Primary DI / UDI-DI
06980305290075
FDA Product Code
QUG
GMDN Term
Air-conduction hearing aid, in-the-ear
Device Class
Class II
Regulation Number
874.3305
GUDID distribution status
In Commercial Distribution

Other devices from Shenzhen Cannice Technology Co., Ltd

See all devices from Shenzhen Cannice Technology Co., Ltd →

Properties

  • Over-the-Counter
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No