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G-EO System

by Reha Technology AG

G-EO System is a Class II device made by Reha Technology AG, listed in FDA GUDID since 29 Sep 2016 (UDI-DI 07640174420018), registry data as of 31 May 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 31 May 2026.

Regulatory status

as of registry sync 31 May 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07640174420018 UDI-DI Date29 Sep 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  • Withdrawn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

Generic name
Treadmill/elliptical gait rehabilitation system
Model / reference
G-EO System
Primary DI / UDI-DI
07640174420018
FDA product code
IKK
GMDN term
Treadmill/elliptical gait rehabilitation system
Device class
Class II
Regulation number
890.1925
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code IKK (System, Isokinetic Testing And Evaluation).

Other devices from Reha Technology AG

  • G-Eo

    Class II
  • Armotion

    Class II

Properties

  • Prescription use
  • Premarket exempt
Other properties (13, all answered No)