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Interacoustics Titan

by Interacoustics A/S

Interacoustics Titan is a Class II device made by Interacoustics A/S, listed in FDA GUDID since 28 Jul 2026 (UDI-DI 05711117244557), 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 Number05711117244557 UDI-DI Date28 Jul 2026ListedStatusListed 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  • Withdrawn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
Interacoustics
Generic name
Otoacoustic emission system, battery-powered
Model / reference
Titan
Primary DI / UDI-DI
05711117244557
FDA product code
EWO, GWJ, ETY
GMDN term
Otoacoustic emission system, battery-powered
Device class
Class II
Regulation number
874.1050, 882.1900, 874.1090
GUDID distribution status
In Commercial Distribution

Other devices from Interacoustics A/S

See all devices from Interacoustics A/S →

Properties

  • Serial number
  • Manufacturing date
Other properties (13, all answered No)