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Cionic 10

by Cionic, Inc. 2 variants

Cionic 10 (62000004) is a Class II device made by Cionic, Inc., listed in FDA GUDID since 1 Dec 2022 (UDI-DI G345620000040), 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 NumberG345620000040 UDI-DI Date1 Dec 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Cionic
Generic name
Gait-enhancement electrical stimulation system, external
Model / Ref / Catalog
10, 62000004
Primary DI / UDI-DI
G345620000040
FDA product code
GZI, IPF
GMDN term
Gait-enhancement electrical stimulation system, external
Device class
Class II
Regulation number
882.5810, 890.5850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Gait-enhancement electrical stimulation system, external

Similar devices

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

Other devices from Cionic, Inc.

See all devices from Cionic, Inc. →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)