Identity
- Trade Name
- MindMotion™ GO FDA UDI
- Generic Name
- Virtual-display rehabilitation system, non-supportive, clinical FDA UDI
- Device Name
- MindMotion™ GO is a medical device software used in combination with the Microsoft Kinect v2 and Leap Motion controller that supports the physical rehabilitation of adults in the clinic and at home. The software includes rehabilitation exercises for the upper extremity, trunk, and lower extremity; audio-visual feedback and graphic movement representations for patients; and patient performance metrics for the medical professional. Patient assessment, exercise guidance, and approval by the medical professional is required prior to use. FDA UDI
- Model / Reference
- MMG-01 FDA UDI
- Description
- MindMotion™ GO is a medical device software used in combination with the Microsoft Kinect v2 and Leap Motion controller that supports the physical rehabilitation of adults in the clinic and at home. The software includes rehabilitation exercises for the upper extremity, trunk, and lower extremity; audio-visual feedback and graphic movement representations for patients; and patient performance metrics for the medical professional. Patient assessment, exercise guidance, and approval by the medical professional is required prior to use. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03760272650019 FDA UDI
- FDA Product Code
- QKC FDA UDI
- GMDN Term
- Virtual-display rehabilitation system, non-supportive, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5360 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Virtual-display rehabilitation system, non-supportive, clinical
MindMotion™ GO by MindMaze SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Virtual-display rehabilitation system, non-supportive, clinical.
- REAL Immersive System — PENUMBRA, INC. · Class II
- MES 9000 Muscle Tester — MYOTRONICS-NOROMED, INC. · Class II
- Noromed NT-360 Inclinometer — MYOTRONICS-NOROMED, INC. · Class I
- PABLO Lower Extremity — tyromotion GmbH · Class I
- REAL Immersive System — PENUMBRA, INC. · Class II
- ARIA — Smith & Nephew, Inc. · Class II
- TYMO — tyromotion GmbH · Class I
- VERA — Reflexion Health, Inc. · Class II
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
- MindMaze SA
Sources (1)
- FDA UDI ca78fc1c-e773-4de9-af1d-dde3871f62b9 34 fields · synced Jun 1, 2026