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Audiosync Edge Ai 20 Ric 312

by Starkey Laboratories Inc.

Audiosync Edge Ai 20 Ric 312 is a Class II device made by Starkey Laboratories Inc., listed in FDA GUDID since 29 Nov 2024 (UDI-DI 00840388204290), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840388204290 UDI-DI Date29 Nov 2024ListedStatusListed 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  • Withdrawn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
Audiosync
Generic name
Tinnitus masking application software
Model / reference
AUDIOSYNC EDGE AI 20 RIC 312
Primary DI / UDI-DI
00840388204290
FDA product code
OSM, KLW
GMDN term
Tinnitus masking application software
Device class
Class II
Regulation number
874.3305, 874.3400
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Air-conduction hearing aid, receiver-in-canalTinnitus masking application software

Other devices from Starkey Laboratories Inc.

See all devices from Starkey Laboratories Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)