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Ultratone Futura Pro (US Specification)

by Ultratone Scientific Instruments Limited

Ultratone Futura Pro (US Specification) (USFPC1) is a Class II device made by Ultratone Scientific Instruments Limited, listed in FDA GUDID since 25 Oct 2016 (UDI-DI 05056119700008), 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 Number05056119700008 UDI-DI Date25 Oct 2016ListedStatusListed 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  • Withdrawn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
Ultratone
Generic name
Multi-modality physical therapy system, simultaneous, professional-use
Model / Ref / Catalog
Futura Pro (US Specification), USFPC1
Primary DI / UDI-DI
05056119700008
FDA product code
IMG
GMDN term
Multi-modality physical therapy system, simultaneous, professional-use
Device class
Class II
Regulation number
890.5860
GUDID distribution status
In Commercial Distribution

Related devices

Category: Physical therapy ultrasound/neuromuscular stimulation system

Similar devices

Other devices filed under FDA product code IMG (Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat).

Properties

  • Serial number
Other properties (14, all answered No)