FDA.reportPublic FDA data

VIVACE ULTRA

Primary DI
G055ABMVIVM121
Brand
VIVACE ULTRA
Company
Aesthetics Biomedical, Inc.
Model
VERSION 1.0
Catalog number
ABMVIVM12
Device description
10 CARTRIDGES CONTAINING 60 NON-INSULATED MICRONEEDLES IN A SQUARE PATTERN
Published
2022-12-30
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
GEIElectrosurgical, Cutting & Coagulation & Accessories
IYOSystem, Imaging, Pulsed Echo, Ultrasonic
OUHSkin Resurfacing Rf Applicator

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEIElectrosurgical, Cutting & Coagulation & AccessoriesGeneral, Plastic Surgery2
IYOSystem, Imaging, Pulsed Echo, UltrasonicRadiology2
OUHSkin Resurfacing Rf ApplicatorGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K221574000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K221574000LUDWIG Electrosurgical DeviceAesthetics Biomedical2022-10-16GEI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
G055ABMVIVM121PrimaryHIBCC0
G055ABMVIVM120Unit of UseHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Intradermal radio-frequency ablation system needle electrodeAn electrical conductor intended to be introduced into the dermal layer of the skin (intradermal) to deliver radio-frequency (RF) current in a monopolar configuration for coagulation/ablation, to treat skin conditions [typically superficial skin lesions (e.g., telangiectasia, cherry angioma, venous lake, skin tags) and/or acne]. It is intended to be used in conjunction with an appropriate RF generator and attached to a probe handle (not included). This is a single-use device.

Regulatory Flags#

DUNS number
033599752
Device count
10
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
G055ABMVIVS020VIVACE ULTRAVERSION 1.0ABMVIVS022022-12-30
G055ABMVIVM031VIVACE ULTRAVERSION 1.0ABMVIVM032022-12-30
G055ABMVIVM041VIVACE ULTRAVERSION 1.0ABMVIVM042022-12-30
G055ABMVIVM071VIVACE ULTRAVERSION 1.0ABMVIVM072022-12-30
G055ABMVIVM081VIVACE ULTRAVERSION 1.0ABMVIVM082022-12-30
G055ABMVIVM111VIVACE ULTRAVERSION 1.0ABMVIVM112022-12-30
G055ABMVIVU010VIVACE ULTRAVERSION 1.0ABMVIVU012022-12-30
G055ABMVIVM010VIVACE ULTRAVERSION 1.0ABMVIVM012022-12-30
G055ABMVIVM020VIVACE ULTRAVERSION 1.0ABMVIVM022022-12-30
G055ABMVIVM050VIVACE ULTRAVERSION 1.0ABMVIVM052022-12-30
G055ABMVIVM060VIVACE ULTRAVERSION 1.0ABMVIVM062022-12-30
G055ABMVIVM090VIVACE ULTRAVERSION 1.0ABMVIVM092022-12-30
G055ABMVIVM100VIVACE ULTRAVERSION 1.0ABMVIVM102022-12-30
G055ABMVIVR010VIVACE ULTRAVERSION 1.0ABMVIVR012022-12-30
G055ABMVIVS010VIVACE ULTRAVERSION 1.0ABMVIVS012022-12-30
G055ABMVIVM030VIVACE ULTRAVERSION 1.0ABMVIVM032022-12-30
G055ABMVIVM040VIVACE ULTRAVERSION 1.0ABMVIVM042022-12-30
G055ABMVIVM070VIVACE ULTRAVERSION 1.0ABMVIVM072022-12-30
G055ABMVIVM080VIVACE ULTRAVERSION 1.0ABMVIVM082022-12-30
G055ABMVIVM110VIVACE ULTRAVERSION 1.0ABMVIVM112022-12-30

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00840319759073Hayden MedicalHayden Medical, Inc.GEI2026-06-04
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08809306764171VIVA RF ElectrodeSTARMED CO.,LTDGEI2026-06-04
08809306764188VIVA RF ElectrodeSTARMED CO.,LTDGEI2026-06-04
00198506091261ELMED INCORPORATEDELMED INCORPORATEDGEI2026-06-03
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