
Orthoscan, Inc.
Free shipping on orders over $99 · 30-day returns
ORTHOSCAN MOBILE DI MINI C-ARM is an FDA 510(k)-cleared medical device (K113708) manufactured by Orthoscan, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 4, 2012. Regulation: 8.