TRUEdraw Lancing Device, Mini Lancing Device

TRUEdraw Lancing Device, Mini Lancing Device is an FDA 510(k)-cleared medical device (K221072) manufactured by Trividia Health. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 17, 2022. Regulation: 8.