Skip to content

Axon Android

by Exsurgo Limited

Axon Android (100321) is a Class II device made by Exsurgo Limited, listed in FDA GUDID since 16 Aug 2021 (UDI-DI 09413000078510), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number09413000078510 UDI-DI Date16 Aug 2021ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Axon
Generic name
Psychophysiological biofeedback system
Model / Ref / Catalog
Android, 100321
Primary DI / UDI-DI
09413000078510
FDA product code
HCC
GMDN term
Psychophysiological biofeedback system
Device class
Class II
Regulation number
882.5050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Psychophysiological biofeedback system

Similar devices in this category

Other devices filed under Psychophysiological biofeedback system.

Other devices from Exsurgo Limited

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)