Facet 28G Universal Lancet

Facet 28G Universal Lancet is an FDA 510(k)-cleared medical device (K221433) 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 July 14, 2022. Regulation: 8.