ClearanceBrief
510(k) K241790 ยท QAI Powered Microneedle Device

XCELLARISPRO TWIST microneedling device

ApplicantDermaroller GmbH, Wolfenbuettel, DE
DecisionSubstantially Equivalent, Mar 6, 2025
ReceivedJun 21, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K241790

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.