NeatNick Heel Safety Lancet

NeatNick Heel Safety Lancet is an FDA 510(k)-cleared medical device (K223370) manufactured by Facet Technologies, LLC. 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 February 12, 2023. Regulation: 8.