
Heraeus Kulzer, Inc.
Free shipping on orders over $99 · 30-day returns
DENTALON PLUS MODIFICATION is an FDA 510(k)-cleared medical device (K934283) manufactured by Heraeus Kulzer, 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 December 9, 1993. Regulation: 8.