
Hati Dental Ag.
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HA-TI (HAND TITANIUM SCREW) IMPLANT is an FDA 510(k)-cleared medical device (K003045) manufactured by Hati Dental Ag.. 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 11, 2001. Regulation: 8.