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RedRevive TFX LT1000N

by Toefx, Inc.

RedRevive TFX LT1000N is a Class II device made by Toefx, Inc., listed in FDA GUDID since 3 Dec 2025 (UDI-DI 00860012465033), 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 Number00860012465033 UDI-DI Date3 Dec 2025ListedStatusListed 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  • Withdrawn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
RedRevive
Generic name
Blue/red/infrared phototherapy lamp
Model / reference
TFX LT1000N
Primary DI / UDI-DI
00860012465033
FDA product code
ILY
GMDN term
Blue/red/infrared phototherapy lamp
Device class
Class II
Regulation number
890.5500
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ILY (Lamp, Infrared, Therapeutic Heating).

Other devices from Toefx, Inc.

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)