Data / Medical devices / United Kingdom / Aesthetic Technology Ltd
Aesthetic Technology Ltd: FDA-registered device maker in Warrington Cheshire East, United Kingdom, 4 510(k) clearances
Aesthetic Technology Ltd is registered with the FDA (registration 3017140525) in Warrington Cheshire East, United Kingdom. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 4, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017140525
- Address
- Unit 211 Europa Boulevard, Warrington Cheshire East, United Kingdom, WA5 7TN
- Owner or operator
- Aesthetic Technology Ltd. (10062533)
- Roles
- Manufacturer
- First device listed
- June 25, 2020
- Registered through
- 2026
- Brand names listed
- Dermalux Compact MD, Dermalux Flex MD, Dermalux Tri-Wave MD MKII, Dermalux Triwave MD
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Manufacturer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 4, 2024 | K240222 | Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024) | GEX | Substantially Equivalent | Aesthetic Technology, Ltd. | accessdata.fda.gov |
| November 18, 2021 | K212275 | Dermalux Flex MD | OHS | Substantially Equivalent | Aesthetic Technology, Ltd. | accessdata.fda.gov |
| December 16, 2020 | K202028 | dermalux Flex MD | ILY | Substantially Equivalent | Aesthetic Technology, Ltd. | accessdata.fda.gov |
| May 9, 2020 | K200659 | Dermalux Tri-Wave MD | GEX | Substantially Equivalent | Aesthetic Technology, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Light Based Over The Counter Wrinkle Reduction
Updated June 4, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.