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Sign in to claim this brandAesthetic Technology, Ltd.
US
Last updated May 24, 2026
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.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Aesthetic Technology, Ltd. manufacture?
Aesthetic Technology, Ltd. specializes in phototherapy lamps that use blue, red, and infrared light. These devices are primarily designed for medical and aesthetic applications, such as skin rejuvenation, acne treatment, and tissue stimulation. The company’s portfolio includes the Dermalux series, which features multiple models like the Dermalux Tri-Wave MD, Dermalux Flex MD, and their variants, each tailored for specific clinical or patient needs.
Where is Aesthetic Technology, Ltd. based, and how does that affect its regulatory oversight?
Aesthetic Technology, Ltd. is based in the United States, which means its devices fall under FDA regulatory jurisdiction. Since the company’s products are classified as Class II medical devices, they undergo evaluation through pathways like the 510(k) clearance process and the Unique Device Identification (UDI) system to ensure compliance with US medical device regulations.
Which regulatory registries or databases list Aesthetic Technology, Ltd.’s devices?
Aesthetic Technology, Ltd.’s devices are tracked in the FDA’s regulatory databases, specifically through the 510(k) clearance process and the Unique Device Identification (UDI) system. These registries ensure traceability and compliance for Class II devices like the Dermalux series, which are authorised for medical and aesthetic use in the US.
How are Aesthetic Technology, Ltd.’s devices classified under US regulations?
Aesthetic Technology, Ltd.’s devices are classified as Class II medical devices in the US. This classification requires manufacturers to demonstrate that their products are substantially equivalent to a legally marketed predicate device through pathways like the 510(k) clearance, ensuring they meet safety and performance standards before being authorised for use.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 218753736
Catalogue (7)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Dermalux | Flex MD | FDA UDI | Class II | Active |
| Dermalux | Tri-Wave MD MKII | FDA UDI | Class II | Active |
| Dermalux | Flex MD | FDA UDI | Class II | Active |
| Dermalux Tri-Wave MD | K200659 | FDA 510(k) | Class II | Active |
| Dermalux Flex MD | K212275 | FDA 510(k) | Class II | Active |
| Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024) | K240222 | EUDAMEDFDA 510(k) | Class II | Active |
| dermalux Flex MD | K202028 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Aesthetic Technology Ltd Warrington Cheshire East · GB FEI 3017140525