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MyndMove FES System

by Myndtec, Inc. 3 variants

MyndMove FES System (900200) 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 11 Dec 2019 (UDI-DI 00692520002000), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K170564

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00692520002000 UDI-DI Date11 Dec 2019ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK170564 Date30 Aug 2017DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K170564 decided 30 Aug 2017 Active
  • FDA GUDID UDI-DI 00692520002000 listed 11 Dec 2019 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K170564
  2. Listed FDA GUDID 00692520002000

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
MyndMove
Generic name
Physical therapy transcutaneous neuromuscular electrical stimulation system
Model / Ref / Catalog
MyndMove FES System, 900200
Primary DI / UDI-DI
00692520002000
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
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Physical therapy transcutaneous neuromuscular electrical stimulation systemNeuromuscular transmission electrodeNeuromuscular transmission electrode/sensor lead

Cleared under the same submission (K170564)

and 8 more cleared under K170564

Similar devices

Other devices filed under FDA product code IPF (Stimulator, Muscle, Powered).

Other devices from Myndtec, Inc.

See all devices from Myndtec, Inc. →

Properties

  • Prescription use
  • Convenience kit
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)