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FDA 510(k)

TelioCAD Multi

K-Number: K153753 · 2016-04-12

ApplicantIvoclar Vivadent, Inc.
Decision Date2016-04-12
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TelioCAD Multi is a medical device manufactured by Ivoclar Vivadent, Inc.. It received FDA 510(k) clearance on 2016-04-12 under approval number K153753. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TelioCAD Multi?

TelioCAD Multi is a medical device that received FDA 510(k) clearance on 2016-04-12. It is manufactured by Ivoclar Vivadent, Inc.. The 510(k) number is K153753.

When was TelioCAD Multi approved by the FDA?

TelioCAD Multi received FDA 510(k) clearance on 2016-04-12, under approval number K153753.

What company makes TelioCAD Multi?

TelioCAD Multi is manufactured by Ivoclar Vivadent, Inc..

What is the FDA product code for TelioCAD Multi?

The FDA product code for TelioCAD Multi is EBG.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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