
Genteel, LLC
Free shipping on orders over $99 · 30-day returns
Genteel Lancing Device is an FDA 510(k)-cleared medical device (K153670) manufactured by Genteel, 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 May 11, 2016. Regulation: 8.