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FDA 510(k)

ZMATCH BLOCK

K-Number: K083201 · 2009-01-26

ApplicantDentaim Co., Ltd.
Decision Date2009-01-26
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ZMATCH BLOCK is the device name listed in this FDA 510(k) record. The listed applicant is Dentaim Co., Ltd.. It received FDA 510(k) clearance on 2009-01-26 under 510(k) number K083201. 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 ZMATCH BLOCK?

ZMATCH BLOCK is a medical device that received FDA 510(k) clearance on 2009-01-26. The listed applicant is Dentaim Co., Ltd.. The 510(k) number is K083201.

When did ZMATCH BLOCK receive FDA 510(k) clearance?

ZMATCH BLOCK received FDA 510(k) clearance on 2009-01-26, under 510(k) number K083201.

Who is the listed applicant for ZMATCH BLOCK?

The FDA 510(k) record lists Dentaim Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZMATCH BLOCK?

The FDA product code for ZMATCH BLOCK 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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