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NeuroSwitch PL-25-1000

by Control Bionics Incorporated

NeuroSwitch PL-25-1000 is a Class II device made by Control Bionics Incorporated, listed in FDA GUDID since 6 Mar 2018 (UDI-DI 00864267000414), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00864267000414 UDI-DI Date6 Mar 2018ListedStatusListed 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  • Withdrawn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
NeuroSwitch
Generic name
Voice synthesizer/digitizer
Model / reference
PL-25-1000
Primary DI / UDI-DI
00864267000414
FDA product code
ILQ, IQA
GMDN term
Voice synthesizer/digitizer
Device class
Class II
Regulation number
890.3710, 890.3725
GUDID distribution status
In Commercial Distribution

Related devices

Category: Voice synthesizer/digitizer

Similar devices

Other devices filed under FDA product code ILQ (System, Communication, Powered).

Other devices from Control Bionics Incorporated

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)