Identity
- Trade Name
- ReJoyce FDA UDI
- Generic Name
- Virtual-display arm rehabilitation system, non-gravity-compensating FDA UDI
- Device Name
- The ReJoyce is a rehabilitation device intended to increase the strength of muscles and the range of motion of joints of the upper extremities. The ReJoyce helps patients to retrain and condition their muscles by using their hands and arms to play interactive computer games. The activities required by the computer games are similar to tasks used in everyday life, such as pouring a drink or opening a jar. Practicing these motions will help patients to replicate them in real life. FDA UDI
- Model / Reference
- RV10 FDA UDI
- Description
- The ReJoyce is a rehabilitation device intended to increase the strength of muscles and the range of motion of joints of the upper extremities. The ReJoyce helps patients to retrain and condition their muscles by using their hands and arms to play interactive computer games. The activities required by the computer games are similar to tasks used in everyday life, such as pouring a drink or opening a jar. Practicing these motions will help patients to replicate them in real life. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 17540176010002 FDA UDI
- FDA Product Code
- IKK FDA UDI
- GMDN Term
- Virtual-display arm rehabilitation system, non-gravity-compensating 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
No
FDA UDI
Over-the-Counter
Yes
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 arm rehabilitation system, non-gravity-compensating
ReJoyce by Rehabtronics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Virtual-display arm rehabilitation system, non-gravity-compensating.
- SaeboRejoyce — Saebo 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 |
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Manufacturer
- Manufacturer
- Rehabtronics, Inc.
Sources (1)
- FDA UDI f94e5883-392d-4b16-ab20-0ee44637fe7a 34 fields · synced May 30, 2026