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FDA 510(k)

TEMPORARY CROWN AND BRIDGE MATERIAL

K-Number: K060293 · 2006-02-17

ApplicantDentsply International, Inc.
Decision Date2006-02-17
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TEMPORARY CROWN AND BRIDGE MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply International, Inc.. It received FDA 510(k) clearance on 2006-02-17 under 510(k) number K060293. 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 TEMPORARY CROWN AND BRIDGE MATERIAL?

TEMPORARY CROWN AND BRIDGE MATERIAL is a medical device that received FDA 510(k) clearance on 2006-02-17. The listed applicant is Dentsply International, Inc.. The 510(k) number is K060293.

When did TEMPORARY CROWN AND BRIDGE MATERIAL receive FDA 510(k) clearance?

TEMPORARY CROWN AND BRIDGE MATERIAL received FDA 510(k) clearance on 2006-02-17, under 510(k) number K060293.

Who is the listed applicant for TEMPORARY CROWN AND BRIDGE MATERIAL?

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

What is the FDA product code for TEMPORARY CROWN AND BRIDGE MATERIAL?

The FDA product code for TEMPORARY CROWN AND BRIDGE MATERIAL 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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