dermalux Flex MD— 510(k) K202028

Substantially Equivalent

Aesthetic Technology, Ltd.

FDA 510(k) clearance K202028 for dermalux Flex MD, Substantially Equivalent on 2020-12-16. Applicant: Aesthetic Technology, Ltd..

Clearance details

Applicant: Aesthetic Technology, Ltd.
Product code: Code ILY
Advisory panel: Physical Medicine
Date received: 2020-07-22
Decision date: 2020-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warrington, GB

Download summary PDF View on FDA.gov ↗

Adverse events under product code ILY

product code ILY

Death: 3
Total: 3

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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