Skip to content

Interacoustics Viot Suite

by Interacoustics A/S

Interacoustics Viot Suite is a Class I device made by Interacoustics A/S, listed in FDA GUDID since 6 Dec 2022 (UDI-DI 05711117199765), 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 Number05711117199765 UDI-DI Date6 Dec 2022ListedStatusListed 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  • Withdrawn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
Camera application software
Model / reference
Viot Suite
Primary DI / UDI-DI
05711117199765
FDA product code
ERA
GMDN term
Camera application software
Device class
Class I
Regulation number
874.4770
GUDID distribution status
In Commercial Distribution

Related devices

Category: Camera application software

Similar devices

Other devices filed under FDA product code ERA (Otoscope).

Other devices from Interacoustics A/S

See all devices from Interacoustics A/S →

Properties

  • Premarket exempt
Other properties (14, all answered No)