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Aesthetic Technology, Ltd.

Active in EUDAMED

United Kingdomfrom SRN EUDAMED SRN GB-MF-000033533

Aesthetic Technology, Ltd. is a medical device manufacturer based in the United Kingdom, with 11 devices listed in EUDAMED, FDA 510(k) and FDA GUDID (FDA Class II; EU Class IIa) as of 13 Nov 2026.

Devices
11
Registrations
EUDAMED

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • EUDAMED 5
  • FDA 510(k) 4
  • FDA GUDID 3

A device listed in two registries counts in both.

Device classes
  • FDA Class II 7
  • EU Class IIa 4
Top EMDN categories
Sites and related companies
Identifiers
  • EUDAMED SRN GB-MF-000033533
  • DUNS 218753736

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor

What Aesthetic Technology, Ltd. makes

Aesthetic Technology, Ltd. manufactures blue, red, and infrared phototherapy lamps designed for medical and aesthetic applications, including devices like the Dermalux series and its variants. These products are intended for procedures such as skin rejuvenation, acne treatment, and tissue stimulation, with models tailored for different clinical settings and patient needs.

The company’s portfolio is regulated under Class II medical devices in the US, with devices authorised through FDA pathways including 510(k) clearances and the Unique Device Identification (UDI) system. All listed products are tracked within the FDA’s regulatory databases for compliance and traceability.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue11

Newest first, rows 1-11 of 11

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  • Dermalux Ref 1000023

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Dermalux Ref 1000033

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Dermalux Ref 1000035

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Dermalux Ref 1000015

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • Dermalux Flex MD

    Listed Registry: GUDID Class:II

  • Dermalux Tri-Wave MD MKII

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Dermalux Flex MD

    Listed Registry: GUDID Class:II

  • Dermalux Tri-Wave MD Ref K200659

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Dermalux Flex MD Ref K212275

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024) Ref K240222

    Active Regimes: CE MDD 510(k) Registry: EUDAMED510(k) Class:II

  • dermalux Flex MD Ref K202028

    Active Regimes: CE MDD 510(k) Registry: 510(k) Class:II

Rows 1-11 of 11

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
GB-MF-000033533
DUNS number
218753736
EU VAT number
GB159249674
EUDAMED status
Active
EUDAMED registered name
Aesthetic Technology Ltd
EUDAMED abbreviated name
ATL
Registered address
Unit 211, Europa Boulevard, WA5 7TN, Warrington, United Kingdom (ex Northern Ireland)
PRRC contact
George Gray(public in EUDAMED)

Sites1

Frequently asked questions

How many devices does Aesthetic Technology, Ltd. have in the registry?

The registry currently lists 11 devices for Aesthetic Technology, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Aesthetic Technology, Ltd.'s devices?

Among its 11 most recently registered devices, Aesthetic Technology, Ltd. has devices listed in EUDAMED (5 devices), FDA 510(k) (4 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Aesthetic Technology, Ltd.'s devices fall under?

Among its 11 most recently registered devices, the classes recorded for Aesthetic Technology, Ltd.'s devices are Class IIa and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Aesthetic Technology, Ltd. in the registry?

The most recently registered devices listed for Aesthetic Technology, Ltd. include Dermalux, Dermalux Flex MD, Dermalux Tri-Wave MD MKII and Dermalux Tri-Wave MD.

Generated automatically from registry data and not verified by a human reviewer.