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FDA 510(k)

VENEER CEMENT

K-Number: K923328 · 1992-09-09

ApplicantDentsply Intl.
Decision Date1992-09-09
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VENEER CEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1992-09-09 under 510(k) number K923328. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENEER CEMENT?

VENEER CEMENT is a medical device that received FDA 510(k) clearance on 1992-09-09. The listed applicant is Dentsply Intl.. The 510(k) number is K923328.

When did VENEER CEMENT receive FDA 510(k) clearance?

VENEER CEMENT received FDA 510(k) clearance on 1992-09-09, under 510(k) number K923328.

Who is the listed applicant for VENEER CEMENT?

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

What is the FDA product code for VENEER CEMENT?

The FDA product code for VENEER CEMENT is EMA.

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Related Devices (Code: EMA)

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.

K262983EsTemp ImplantSpident Co., Ltd.K254201Any-CemMediclus Co., Ltd.K261937PacTemp Automix NEThe Belport Company Inc., DBA Gingi-PakK261166DIA-CEMDiaDent Group InternationalK254109G-CEM UNIVERSALGC America, Inc.K253337REGEN Bioactive CementInter-Med, Inc.

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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