Omnilux Eye Brightener

GUDID 05060534510814

Omnilux Eye Brightener- Mini LED Patch to treat facial wrinkles

I-SMART DEVELOPMENTS LIMITED

Cosmetic red-light phototherapy system, home-use
Primary Device ID05060534510814
NIH Device Record Key6ce0e361-fb23-4a0a-a2fa-6188ce337902
Commercial Distribution StatusIn Commercial Distribution
Brand NameOmnilux Eye Brightener
Version Model NumberTN2189
Company DUNS223616320
Company NameI-SMART DEVELOPMENTS LIMITED
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS105060534510814 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OHSLight Based Over The Counter Wrinkle Reduction

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-11-03
Device Publish Date2023-10-26

Devices Manufactured by I-SMART DEVELOPMENTS LIMITED

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05060534510685 - Luma Blemish2023-11-03 Luma Blemish- Mini LED Patch to treat mild to moderate acne vulgaris

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