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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 the device name listed in this FDA 510(k) record. The listed applicant is Ivoclar Vivadent, Inc.. It received FDA 510(k) clearance on 2016-04-12 under 510(k) 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. The listed applicant is Ivoclar Vivadent, Inc.. The 510(k) number is K153753.

When did TelioCAD Multi receive FDA 510(k) clearance?

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

Who is the listed applicant for TelioCAD Multi?

The FDA 510(k) record lists Ivoclar Vivadent, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TelioCAD Multi?

The FDA product code for TelioCAD Multi is EBG.

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Related Devices (Code: EBG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261261Dura-ArchHangzhou SHINING3D Dental Technology Co., Ltd.K253380“FLNT Base” and “FLNT Temp”Liaoning Upcera Co., Ltd.K251271TempFIT Temporary Crown and Bridge ResinRizhao Huge Biomaterials Company, Ltd.K243370DentaTOOTHAsiga Pty, Ltd.K243621Evoblock, PerléonEvoden Indústria Comércio Importação E ExportaçãoK243951TEMP MASTER, PMMA-based dental resinTaiwan Dental Materials Co., Ltd.

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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