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STARKEY MUSE I1600 RIC 312t

by Starkey Laboratories Inc. 2 variants

STARKEY MUSE I1600 RIC 312t (64247-7) is a Class II device made by Starkey Laboratories Inc., listed in FDA GUDID since 10 Jan 2017 (UDI-DI 00842318116086), 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 Number00842318116086 UDI-DI Date10 Jan 2017ListedStatusListed 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  • Withdrawn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
Starkey
Generic name
Tinnitus masking application software
Model / Ref / Catalog
MUSE I1600 RIC 312t, 64247-7
Primary DI / UDI-DI
00842318116086
FDA product code
KLW, OSM
GMDN term
Tinnitus masking application software
Device class
Class II
Regulation number
874.3400, 874.3305
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)