FDA UDI In Commercial Distribution 🇺🇸 United States

MediLight

DI: 00860009525146 · Model: 2.0 · MEDICREATIONS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MediLight
Primary DI
00860009525146
Version / Model
2.0
Company Name
MEDICREATIONS LLC
Labeler DUNS
106075496
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-11
Public Version
1
Public Version Date
2026-02-19
Public Version Status
New
Public Device Record Key
4794cba9-70e9-49eb-80a4-8a0d0b7ceddc

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

GMDN Terms

Code Name
58935 Intense pulsed light skin surface treatment system

Identifiers

Type ID
Primary 00860009525146

Premarket Submissions

Submission Number Supplement Number
K231952 000