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MyndMove Mobile Cart

by Myndtec, Inc.

MyndMove Mobile Cart (920276) is a Class II device made by Myndtec, Inc., cleared under FDA 510(k) K212149 on 3 Mar 2022 (1 earlier submission) and listed in FDA GUDID since 19 Aug 2022 (UDI-DI 00692520202769), 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

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00692520202769 UDI-DI Date19 Aug 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK212149 Date3 Mar 2022DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K212149 decided 3 Mar 2022 Active· +1 more in the status table
  • FDA GUDID UDI-DI 00692520202769 listed 19 Aug 2022 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K170564
  2. Cleared FDA 510(k) K212149
  3. Listed FDA GUDID 00692520202769

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  • Withdrawn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 Mobile Cart, 920276
Primary DI / UDI-DI
00692520202769
510(k) Number
FDA product code
GZI
GMDN term
Physical therapy transcutaneous neuromuscular electrical stimulation system
Device class
Class II
Regulation number
882.5810
GUDID distribution status
In Commercial Distribution

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

Cleared under the same submission (K212149)

Similar devices

Other devices filed under FDA product code GZI (Stimulator, Neuromuscular, External Functional).

Other devices from Myndtec, Inc.

See all devices from Myndtec, Inc. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)