MyndMove
MyndMove (910165) is a Class II device made by Myndtec, Inc., cleared under FDA 510(k) K170564 on 30 Aug 2017 and listed in FDA GUDID since 24 Oct 2017 (UDI-DI 06925209101652), active (FDA 510(k)), not in commercial distribution (GUDID) as of 1 Jun 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06925209101652 | Date24 Oct 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK170564 | Date30 Aug 2017 | StatusActive |
Official records
- AccessGUDID record 06925209101652
- FDA 510(k) database K170564
Across registries
- FDA 510(k) K170564 decided 30 Aug 2017 Active
- FDA GUDID UDI-DI 06925209101652 listed 24 Oct 2017 Listed
Timeline
- Cleared FDA 510(k) K170564
- Listed FDA GUDID 06925209101652
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Physical therapy transcutaneous neuromuscular electrical stimulation system
- Model / Ref / Catalog
- MyndMove Functional Electrical Stimulator, 910165
- Primary DI / UDI-DI
- 06925209101652
- 510(k) Number
- 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
- Not in Commercial Distribution
- MRI safety
- MR Unsafe
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Other devices filed under FDA product code IPF (Stimulator, Muscle, Powered).
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- Tai Sheng Neox Powered Muscle Stimulator by Tai Sheng Electrical Machinery Co., Ltd.
- EMPI MODEL 710, NMS by Empi
- Interstim 100 System by Buckman Co., Inc.
- Verimed Myo/Prems by Verimed Holdings, Inc.
- NEUROTECH-4 Program Neuromuscular Stimulator 281 by Neurotech, Inc.