U.S. FDA Clears Dermalogica’s Next-Generation PRO Pen Microneedling System

The U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for Dermalogica’s PRO Pen Microneedling System as a Class II medical device.
The U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for Dermalogica’s PRO Pen Microneedling System as a Class II medical device.