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FDA 510(k)

TURKOM-CERA

K-Number: K060860 · 2006-05-19

ApplicantDental Suppliers of America, Inc.
Decision Date2006-05-19
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TURKOM-CERA is the device name listed in this FDA 510(k) record. The listed applicant is Dental Suppliers of America, Inc.. It received FDA 510(k) clearance on 2006-05-19 under 510(k) number K060860. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TURKOM-CERA?

TURKOM-CERA is a medical device that received FDA 510(k) clearance on 2006-05-19. The listed applicant is Dental Suppliers of America, Inc.. The 510(k) number is K060860.

When did TURKOM-CERA receive FDA 510(k) clearance?

TURKOM-CERA received FDA 510(k) clearance on 2006-05-19, under 510(k) number K060860.

Who is the listed applicant for TURKOM-CERA?

The FDA 510(k) record lists Dental Suppliers of America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TURKOM-CERA?

The FDA product code for TURKOM-CERA is EIH.

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Related Devices (Code: EIH)

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.

K262074Any-ZircosMediclus Co., Ltd.K262239Obsidian® Press Over ZirconiaPrismatik Dentalcraft, Inc.K261046Dental Zirconia Blank & Coloring LiquidHunan Qinghao Puzhong Technology Co., Ltd.K262195Dandy Ceramic Stain and GlazeZima International Inc., dba DandyK260918Zolid LunarisAmann Girrbach AGK260859Rosetta SM, Rosetta SPHass Corp.

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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