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Atlantis Components, Inc.
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ATLANTIS ABUTMENT FOR 3I CERTAIN MICRO MINI; GEMINI AND GEMINI+ ABUTMENT is an FDA 510(k)-cleared medical device (K062197) manufactured by Atlantis Components, 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 February 27, 2007. Regulation: 8.