MyndMove 2.0 MyndMove FES Stimulator
MyndMove 2.0 MyndMove FES Stimulator (920165) is a Class II device made by Myndtec, Inc., listed in FDA GUDID since 19 Aug 2022 (UDI-DI 00692520201656), 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 | Number00692520201656 | Date19 Aug 2022 | StatusListed |
Official records
- AccessGUDID record 00692520201656
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- MyndMove 2.0
- Generic name
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Model / Ref / Catalog
- MyndMove FES Stimulator, 920165
- Primary DI / UDI-DI
- 00692520201656
- FDA product code
- IPF, GZI
- GMDN term
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Device class
- Class II
- Regulation number
- 890.5850, 882.5810
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Similar devices
Other devices filed under FDA product code IPF (Stimulator, Muscle, Powered).
- STIWELL MED4 by Otto Bock Austria
- MODEL 1000 by Verite
- BIONICARE STIMULATOR BIO-1 by Murray Electronics
- BX-200 SC by Bloomex International, Inc.
- GV 11 (TM), MODEL 9700 by Medical Devices, Inc.
- DYNATRON 100 PLUS by Dynatronics Research Corp.
- STELLA BIO by Egzotech Sp. Z O. O.
- eMVFit (MVF-10M) by Weero Co., Ltd.
- CONTROL SOLUTIONS, INC., MODEL CS3102 HVG by Control Solutions, Inc.
- MS-108, POWERED MUSCLE STIMULATOR by Electro Med Supply, Inc.