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GN ReSound 23119700

by Gn Hearing A/S

GN ReSound 23119700 is a Class II device made by Gn Hearing A/S, listed in FDA GUDID since 7 Mar 2024 (UDI-DI 05708296336531), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05708296336531 UDI-DI Date7 Mar 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  • Withdrawn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
GN ReSound
Generic name
Air-conduction hearing aid, canal
Model / reference
23119700
Primary DI / UDI-DI
05708296336531
FDA product code
OSM, KLW
GMDN term
Air-conduction hearing aid, canal
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, canal

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Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)