RedRevive

GUDID 00860012465033

ToeFX Inc

Blue/red/infrared phototherapy lamp
Primary Device ID00860012465033
NIH Device Record Key91738405-9dd0-4e9a-a746-57b21facbae5
Commercial Distribution StatusIn Commercial Distribution
Brand NameRedRevive
Version Model NumberTFX LT1000N
Company DUNS202099070
Company NameToeFX Inc
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100860012465033 [Primary]

FDA Product Code

ILYLamp, Infrared, Therapeutic Heating

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-12-11
Device Publish Date2025-12-03

Devices Manufactured by ToeFX Inc

00860012465019 - FungalBlue2025-12-11 A temporary skin/nail-marking pen used by clinicians to outline areas of interest on the nail, including regions they plan to as
00860012465033 - RedRevive2025-12-11
00860012465033 - RedRevive2025-12-11
00086001245602 - TFX-LT2000 Therapy Light2024-11-25 Light therapy device for onychomycosis

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