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MyndMove

FDA UDI

Class II (US FDA UDI)

by Myndtec, Inc.

Identity

Trade Name
MyndMove FDA UDI
Generic Name
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
Model / Reference
MyndMove Mobile Cart FDA UDI

Identifiers

Catalog Number
920276 FDA UDI
Primary DI / UDI-DI
00692520202769 FDA UDI
510(k) Number
K170564 FDA UDI
K212149 FDA UDI
FDA Product Code
GZI FDA UDI
GMDN Term
Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

MyndMove by Myndtec, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neuromuscular transmission electrode/sensor lead.

Cleared under the same submission

K170564 also covers:

K212149 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Myndtec, Inc.

Sources (1)

  • FDA UDI 9473c86d-fd78-456e-823a-c3d97fd554cd 34 fields · synced May 30, 2026