DeviceClearance

PRO Pen Microneedling System (6883)— 510(k) K243800

Substantially Equivalent

Dermalogica, LLC

FDA 510(k) clearance K243800 for PRO Pen Microneedling System (6883), Substantially Equivalent on 2025-08-25. Applicant: Dermalogica, LLC.

Clearance details

Applicant
Dermalogica, LLC
Product code
Code QAI
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Carson, CA, US
Download summary PDFView on FDA.gov ↗

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