Aesthetic Technology, Ltd.

Aesthetic Technology, Ltd. holds 4 FDA 510(k) medical device clearances, first cleared 2020, most recent 2024.

Top product codes for Aesthetic Technology, Ltd.

Recent clearances by Aesthetic Technology, Ltd.

K240222 — Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024)Code GEX·2024-06-04
K212275 — Dermalux Flex MDCode OHS·2021-11-18
K202028 — dermalux Flex MDCode ILY·2020-12-16
K200659 — Dermalux Tri-Wave MDCode GEX·2020-05-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.