MyoPro Motion G Left - 25920 rev1
by Myomo, Inc.
MyoPro Motion G Left - 25920 rev1 is a Class II device made by Myomo, Inc., listed in FDA GUDID since 1 Apr 2017 (UDI-DI 00855846007092), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00855846007092 | Date1 Apr 2017 | StatusListed |
Official records
- AccessGUDID record 00855846007092
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- MyoPro
- Generic name
- Psychophysiological biofeedback system
- Model / Ref / Catalog
- Motion G Left - 25920 rev1, 25920
- Primary DI / UDI-DI
- 00855846007092
- FDA product code
- HCC, IQI, IRE, IQZ
- GMDN term
- Psychophysiological biofeedback system
- Device class
- Class II
- Regulation number
- 882.5050, 890.3475, 890.3420
- GUDID distribution status
- In Commercial Distribution
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