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Axon

FDA UDI

Class II (US FDA UDI)

by Exsurgo Limited

Identity

Trade Name
Axon FDA UDI
Generic Name
Psychophysiological biofeedback system FDA UDI
Device Name
Neurofeedback Software Application for Android FDA UDI
Model / Reference
Android FDA UDI
Description
Neurofeedback Software Application for Android FDA UDI

Identifiers

Catalog Number
100321 FDA UDI
Primary DI / UDI-DI
09413000078510 FDA UDI
FDA Product Code
HCC FDA UDI
GMDN Term
Psychophysiological biofeedback system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5050 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Psychophysiological biofeedback system

Axon by Exsurgo Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Psychophysiological biofeedback system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Exsurgo Limited

Sources (1)

  • FDA UDI 830021a2-4963-4818-b543-b4c688a98e39 35 fields · synced Jun 1, 2026