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Sonic 226428

by Sbo Hearing A/S

Sonic 226428 is a hearing aid/implant system remote control (FDA Class II) made by Sbo Hearing A/S, listed in FDA GUDID since 22 Apr 2021 (UDI-DI 05714464012053), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05714464012053 UDI-DI Date22 Apr 2021ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Sonic
Generic name
Hearing aid/implant system remote control
Model / reference
226428
Primary DI / UDI-DI
05714464012053
FDA product code
OSM, KLW
GMDN term
Hearing aid/implant system remote control
Device class
Class II
Regulation number
874.3305, 874.3400
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Similar devices in this category

Other devices filed under Hearing aid/implant system remote control.

Other devices from Sbo Hearing A/S

  • Gpl

    Class IIa
  • Amplifon

    Class IIa
  • Hhm

    Class IIa
  • ViO

    Class IIa

See all devices from Sbo Hearing A/S →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)