Microneedling Adverse Event Reports in FDA’s MAUDE, by Brand
The FDA’s MAUDE adverse event database holds 60 reports filed under QAI, the product code for microneedling devices, in data last updated by openFDA on September 29, 2026. Searched by brand, Dr. Pen has 2 reports, Dermapen 2, SkinPen 13, and Derminator 3, which are filed under a different product code. None of these numbers…