
Azary Technologies, LLC
Free shipping on orders over $99 · 30-day returns
BRUGES DISTRACTION - ANCHORING - OSTEOSYNTHESIS SYSTEM is an FDA 510(k)-cleared medical device (K013672) manufactured by Azary Technologies, LLC. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 7, 2002. Regulation: 8.