Aesthetic Technology, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Aesthetic Technology, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Dermalux Tri-Wave MD MKII (1000021), Dermalux Flex MD, dermalux Flex MD
4
Total
4
Cleared
0
Denied
Aesthetic Technology, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Warrington, GB.
Latest FDA clearance: Jun 2024. Active since 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Aesthetic Technology, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Richard Hamer Associates, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Aesthetic Technology, Ltd.
4 devices