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Align receives FDA 510(k) clearance for Invisalign Palatal Expander System

Align receives FDA 510(k) clearance for Invisalign Palatal Expander System

Align Technology announced that the U.S. Food and Drug Administration has cleared Align’s Invisalign Palatal Expander System for commercial availability in the U.S. The FDA 510(k) clearance is for broad patient applicability, including growing children, teens, and adults.

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