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Axonics 1401

by Axonics Modulation Technologies, Inc. 2 variants

Axonics 1401 is a Class III device made by Axonics Modulation Technologies, Inc., listed in FDA GUDID since 23 Sep 2019 (UDI-DI 10810005340387), 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 Number10810005340387 UDI-DI Date23 Sep 2019ListedStatusListed 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  • Withdrawn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
Axonics
Generic name
Implant battery charger
Model / Ref / Catalog
1401
Primary DI / UDI-DI
10810005340387
FDA product code
QON, EZW
GMDN term
Implant battery charger
Device class
Class III
Regulation number
876.5270
GUDID distribution status
In Commercial Distribution

Related devices

Category: Implant battery charger

Similar devices

Other devices filed under FDA product code EZW.

Other devices from Axonics Modulation Technologies, Inc.

  • Axonics 4101

    Class III

  • Axonics 1401

    Class III

  • Axonics 5101

    Class III

  • Axonics FFG-01 Open recall

    Class III

See all devices from Axonics Modulation Technologies, Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)