Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human

Tokuyama America, Inc.
Free shipping on orders over $99 · 30-day returns
BISTITE II DC is an FDA 510(k)-cleared medical device (K011685) manufactured by Tokuyama America, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 30, 2001. Regulation: 8.