Identity
- Trade Name
- REOGO FDA UDI
- Generic Name
- Virtual-display rehabilitation system, powered-support, upper-limb FDA UDI
- Device Name
- The ReoGoTM therapy platform is a computerized robotics-based system for retraining patients with motor limitations, recovering from CVA or other neuromuscular conditions. The Motorika ReoGo™ System is rehabilitative exercise device intended for medical purposes, such as to measure, evaluate, and increase the strength of muscles and the range of motion of joints specifically designed to prevent the adhesion and contracture of joints, to improve the patients’ range of motion and functional capabilities of the upper extremity. FDA UDI
- Model / Reference
- 09 FDA UDI
- Description
- The ReoGoTM therapy platform is a computerized robotics-based system for retraining patients with motor limitations, recovering from CVA or other neuromuscular conditions. The Motorika ReoGo™ System is rehabilitative exercise device intended for medical purposes, such as to measure, evaluate, and increase the strength of muscles and the range of motion of joints specifically designed to prevent the adhesion and contracture of joints, to improve the patients’ range of motion and functional capabilities of the upper extremity. FDA UDI
Identifiers
- Catalog Number
- REOGO005SYS FDA UDI
- Primary DI / UDI-DI
- 07290017844114 FDA UDI
- FDA Product Code
- IKK FDA UDI
- GMDN Term
- Virtual-display rehabilitation system, powered-support, upper-limb FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.1925 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Virtual-display rehabilitation system, powered-support, upper-limb
Reogo by Motorika Medical (israel) Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Virtual-display rehabilitation system, powered-support, upper-limb.
- Heaxel — HEALTH PIXEL SRL · Class II
- ®Fourier — Shanghai Fourier Intelligence Co., LTD · Class II
- InMotion ARM/HAND — BIONIK, INC. · Class II
- BURT — BARRETT TECHNOLOGY, LLC · Class II
- DIEGO — tyromotion GmbH · Class I
- Gloreha Active Package — IDROGENET SRL · Class I
- rebless planar — H ROBOTICS INC. · Class II
- Gloreha Professional 2 — IDROGENET SRL · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Motorika Medical (israel) Ltd
Sources (1)
- FDA UDI dbca90c1-356e-434c-8cfe-c095a9143f36 34 fields · synced May 30, 2026