MediYag

GUDID 00860009525115

MEDICREATIONS LLC

Dermatological frequency-doubled solid-state laser system
Primary Device ID00860009525115
NIH Device Record Key556a7c40-0bdd-4f47-ad93-c71cdab01de4
Commercial Distribution StatusIn Commercial Distribution
Brand NameMediYag
Version Model Number2.0
Company DUNS106075496
Company NameMEDICREATIONS LLC
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 Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100860009525115 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-02-19
Device Publish Date2026-02-11

Devices Manufactured by MEDICREATIONS LLC

00860009525108 - MediSpa2026-02-19
00860009525115 - MediYag2026-02-19
00860009525115 - MediYag2026-02-19
00860009525122 - MediDiode2026-02-19
00860009525146 - MediLight2026-02-19

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