
Neocis, Inc.
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Neocis Guidance System (NGS) with Yomi Plan v2.0 is an FDA 510(k)-cleared medical device (K202264) manufactured by Neocis, 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 3, 2020. Regulation: 8.