Facet Aurora Reusable Lancet Base

Facet Aurora Reusable Lancet Base is an FDA 510(k)-cleared medical device (K232912) 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 January 24, 2024. Regulation: 8.