Waya Rehab 1
Waya Rehab 1 is a Class II device made by Wellovate, LLC, listed in FDA GUDID since 3 Feb 2025 (UDI-DI G741WHREHABV10), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberG741WHREHABV10 | Date3 Feb 2025 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Waya Rehab
- Generic name
- Biomechanical function analysis/interactive rehabilitation system
- Model / reference
- 1
- Primary DI / UDI-DI
- G741WHREHABV10
- FDA product code
- ISD
- GMDN term
- Biomechanical function analysis/interactive rehabilitation system
- Device class
- Class II
- Regulation number
- 890.5360
- GUDID distribution status
- In Commercial Distribution
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