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NeoTone N-0242-B

by Magic Race LLC

NeoTone N-0242-B is a Class II device made by Magic Race LLC, listed in FDA GUDID since 8 Jan 2017 (UDI-DI 00864618000353), 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 Number00864618000353 UDI-DI Date8 Jan 2017ListedStatusListed 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  • Withdrawn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
NeoTone
Generic name
Physical therapy transcutaneous electrical stimulation system, line-powered
Model / reference
N-0242-B
Primary DI / UDI-DI
00864618000353
FDA product code
IPF
GMDN term
Physical therapy transcutaneous electrical stimulation system, line-powered
Device class
Class II
Regulation number
890.5850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Physical therapy transcutaneous electrical stimulation system, line-powered

Similar devices

Other devices filed under FDA product code IPF (Stimulator, Muscle, Powered).

Other devices from Magic Race LLC

See all devices from Magic Race LLC →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)