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FDA 510(k) K153753, TelioCAD Multi, by Ivoclar Vivadent, Inc.

FDA 510(k) K153753, TelioCAD Multi, by Ivoclar Vivadent, Inc.

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510(K) Number: K153753
Device Name: TelioCAD Multi
Manufacturer: Ivoclar Vivadent, Inc.
Device Classification Name: crown and bridge, temporary, resin
Regulation Number: 872.3770
Classification Product Code: EBG
Date Received: 12/29/2015
Decision Date: 04/12/2016
Regulation Medical Specialty: Dental
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