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InnoWave IWULTRA

by Medisafe UK Limited

InnoWave IWULTRA is a Class I device made by Medisafe UK Limited, listed in FDA GUDID since 31 Mar 2021 (UDI-DI 00724995152734), 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 Number00724995152734 UDI-DI Date31 Mar 2021ListedStatusListed 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  • Withdrawn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
InnoWave
Generic name
Ultrasonic-cleaning water bath
Model / Ref / Catalog
IWULTRA
Primary DI / UDI-DI
00724995152734
FDA product code
FLG
GMDN term
Ultrasonic-cleaning water bath
Device class
Class I
Regulation number
880.6150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ultrasonic-cleaning water bath

Similar devices

Other devices filed under FDA product code FLG (Cleaner, ultrasonic, medical instrument).

Other devices from Medisafe UK Limited

See all devices from Medisafe UK Limited →

Properties

  • Over-the-counter
  • Premarket exempt
  • Manufacturing date
Other properties (12, all answered No)