Levanta Plus

GUDID 08059173396535

QUANTA SYSTEM SPA

Dermatological frequency-doubled solid-state laser system
Primary Device ID08059173396535
NIH Device Record Key86bcb205-eccb-4807-bf70-bc6f8cb347ce
Commercial Distribution StatusIn Commercial Distribution
Brand NameLevanta Plus
Version Model NumberPCMS00356
Company DUNS436045833
Company NameQUANTA SYSTEM SPA
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
GS108059173396535 [Primary]

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 Date2025-12-05
Device Publish Date2025-11-27

Devices Manufactured by QUANTA SYSTEM SPA

08059173396535 - Levanta Plus2025-12-05
08059173396535 - Levanta Plus2025-12-05
08059173392186 - Litho EVO2025-10-07
08059173396375 - Echo2024-07-01
08033945936938 - Laserlith I-dust 2024-05-23 Manufactured for Edap TMS
08059173396474 - Karma 2023-12-21
08059173396399 - Rosso2023-06-23
08059173396405 - Rosso2023-06-23
08033945934767 - Quantabella2023-06-16

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