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FDA 510(k)

SPEEDCEM

K-Number: K091019 · 2009-06-04

ApplicantIvoclar Vivadent, Inc.
Decision Date2009-06-04
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SPEEDCEM 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 2009-06-04 under 510(k) number K091019. 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 SPEEDCEM?

SPEEDCEM is a medical device that received FDA 510(k) clearance on 2009-06-04. The listed applicant is Ivoclar Vivadent, Inc.. The 510(k) number is K091019.

When did SPEEDCEM receive FDA 510(k) clearance?

SPEEDCEM received FDA 510(k) clearance on 2009-06-04, under 510(k) number K091019.

Who is the listed applicant for SPEEDCEM?

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 SPEEDCEM?

The FDA product code for SPEEDCEM 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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