OMNIMAX S4

Primary DI
07290110240042
Brand
OMNIMAX S4
Company
SharpLight Technologies Ltd.
Model
OMNIMAX-S4
Device description
The Dermatologic Treatment Systems (DTS) device family and optional hand pieces, including Intensive Pulse Light (IPL) Infrared light (IR) and Laser light technologies for dermatological treatments by delivery of energy to the human skin.
Published
2023-05-21
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information

Product Codes#

Code, Name table
CodeName
GEXPowered Laser Surgical Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEXPowered Laser Surgical InstrumentGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K111303000
K233304000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K111303000DERMATOLOGICAL TREATMENT DEVICE FAMILYSharplight Technologies, Ltd.2011-12-21GEX
K233304000Omnimax S3, Omnimax S4Sharplight Technologies, Ltd.2023-12-22GEX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07290110240042PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07290110240042072901102400427290110240042

GMDN Terms#

Term, Definition table
TermDefinition
Dermatological solid-state laser systemA mains electricity (AC-powered) device assembly in which input energy (e.g., flashlamp, diode laser) is used to excite a glass/crystal rod, or a fibre doped with a glass/crystal element (known as fibre laser), to emit a high-power laser beam intended to incise, excise, ablate, and vaporize soft tissues for dermatological applications such as skin resurfacing, acne treatment, and/or lesion/hair/tattoo removal; some types may also be used for coagulation/haemostasis procedures. It typically includes a light source, laser beam delivery/positioning device(s), user interface, and controls/foot-switch; it does not include frequency-doubling technology.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
533979399
Device count
1
Serial number
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07290110240035OMNIMAX S3OMNIMAX-S32023-05-21
07290110240073Rapid PeelRAPID–PEEL2023-05-22
07290110240127Rapid VanishRAPID-VANISH2023-05-22
07290110240134Rapid QSRAPID-QS2023-05-22
07290110240059Rapid TightRAPID–TIGHT2023-05-22
07290110240110Rapid DPCRAPID-DPC2023-05-22

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08800020109668Edge HandpieceJeisys Medical Inc.GEX2026-07-16
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08800020109682Edge Guide TipJeisys Medical Inc.GEX2026-07-16
08800020109699Edge Guide TipJeisys Medical Inc.GEX2026-07-16