FDA UDI In Commercial Distribution 🇺🇸 United States

Omnilux Eye Brightener

DI: 05060534510814 · Model: TN2189 · I-SMART DEVELOPMENTS LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Omnilux Eye Brightener
Primary DI
05060534510814
Version / Model
TN2189
Company Name
I-SMART DEVELOPMENTS LIMITED
Labeler DUNS
223616320
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-26
Public Version
1
Public Version Date
2023-11-03
Public Version Status
New
Public Device Record Key
6ce0e361-fb23-4a0a-a2fa-6188ce337902

Device Description

Omnilux Eye Brightener- Mini LED Patch to treat facial wrinkles

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OHS Light Based Over The Counter Wrinkle Reduction

GMDN Terms

Code Name
47704 Cosmetic red-light phototherapy system, home-use

Identifiers

Type ID
Primary 05060534510814

Premarket Submissions

Submission Number Supplement Number
K231555 000