FDA 510(k), K173784, Smylic Invisible Clear Aligners

FDA 510(k), K173784, Smylic Invisible Clear Aligners

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510(K) Number: K173784
Device Name: Smylic Invisible Clear Aligners
Manufacturer: Smylio, Inc
Device Classification Name: aligner, sequential
Regulation Number: 872.5470
Classification Product Code: NXC
Date Received: 12/13/2017
Decision Date: 08/23/2018
Regulation Medical Specialty: Dental

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