FDA.reportPublic FDA data

Dermalux

Primary DI
05060762460011
Brand
Dermalux
Company
AESTHETIC TECHNOLOGY LTD
Model
Tri-Wave MD MKII
Catalog number
1000021
Device description
4-Pod LED phototherapy device.
Published
2025-09-02
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
GEXPowered Laser Surgical Instrument
ILYLamp, Infrared, Therapeutic Heating

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEXPowered Laser Surgical InstrumentGeneral, Plastic Surgery2
ILYLamp, Infrared, Therapeutic HeatingPhysical Medicine2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K240222000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K240222000Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024)Aesthetic Technology, Ltd.2024-06-04GEX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
05060762460011PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
05060762460011050607624600115060762460011

GMDN Terms#

Term, Definition table
TermDefinition
Blue/red/infrared phototherapy lampA portable, electrically-powered device designed to emit blue light, red light, and infrared radiation (heating effect) for phototherapy treatment of mild skin disorders (e.g., mild acne), superficial skin wounds, musculoskeletal symptoms (e.g., pain, spasm, stiffness), and/or for cosmetic skin rejuvenation. It may have various designs (e.g., hand-held, book-like, flexible pad for adapting to body areas) and is intended for use in the home or a clinical setting.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Height1087.4Millimeter
Length679.7Millimeter
Weight55Kilogram
Width517.7Millimeter

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
218753736
Device count
1
DM exempt
true
Serial number
true
Manufacturing date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
05060762460028DermaluxFlex MD10000532025-09-02
05060762460080DermaluxFlex MD10001612025-09-02
50607624600118DermaluxTri-Wave MD MKII10000212025-09-02
50607624600286DermaluxFlex MD10000532025-09-02
50607624600804DermaluxFlex MD10001612025-09-02

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00860179001013FUSION PBM Plus LightDentlight Inc.ILY2026-05-27
06974077940016MLKJWeifang Mingliang Electronics Co., Ltd.GEX2026-05-27
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B317KLGEHUF0GIROELTECH KLASER SRLILY2026-05-27
B317KLGUHUF0GIROELTECH KLASER SRLILY2026-05-27
07898672790823Medical SanMEDICAL SAN INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDAGEX2026-05-12
08056389701122EPI-C PLUSESPANSIONE MARKETING SPAGEX2026-04-30
08034108513317DEKA LUXEA PLUSDEKA M.E.L.A. SRLGEX2025-12-16
08052049500326Splendor XBIOS SRLGEX2025-01-16
08052049500333Splendor XBIOS SRLGEX2025-01-16
08052049500340Splendor XBIOS SRLGEX2025-01-16
08052049500357Splendor XBIOS SRLGEX2025-01-16
00851842007623LightScalpelLightscalpel, LLCGEX2023-06-26
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08056389700088E-LIGHT LINEESPANSIONE MARKETING SPAGEX2019-09-03
08057949171553LUMIX ULTRA/PLUSFISIOLINE SRLILY2019-09-02
08057017760276DEKA SMARTXIDE²EL.EN. SPAGEX2019-03-15
08057017760283DEKA SMARTXIDE²EL.EN. SPAGEX2019-03-15
08057017760344DEKA MOTUS AYEL.EN. SPAGEX2019-03-15
08059173390021Youlaser CO2QUANTA SYSTEM SPAGEX2019-01-07
08059173390038Olympus Empower H35 QUANTA SYSTEM SPAGEX2018-12-04
08059173390045Olympus Empower H65QUANTA SYSTEM SPAGEX2018-12-04
08057017760382DEKA SmartXide² TRIO C60HEL.EN. SPAGEX2018-11-26
08057017760399DEKA SmartXide² TRIO C80HEL.EN. SPAGEX2018-11-26
08033945938413Single use Surgical Optical FiberQUANTA SYSTEM SPAGEX2018-09-28