Skip to content

Cionic Dc-100

by Cionic, Inc.

Cionic Dc-100 (DC100) is a Class II device made by Cionic, Inc., listed in FDA GUDID since 26 Jan 2024 (UDI-DI G345DC1000), 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 NumberG345DC1000 UDI-DI Date26 Jan 2024ListedStatusListed 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  • Withdrawn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
DC-100, DC100
Primary DI / UDI-DI
G345DC1000
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

Other devices from Cionic, Inc.

See all devices from Cionic, Inc. →

Properties

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