
Uresil Corp.
Free shipping on orders over $99 · 30-day returns
URESIL ENDOSCOPIC LASER OVERTUBE is an FDA 510(k)-cleared medical device (K901882) manufactured by Uresil Corp.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 26, 1990. Regulation: 8.