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FDA 510(k)

VINTAGE MP PRESS OVER

K-Number: K122614 · 2013-05-16

ApplicantShofu Dental Corporation
Decision Date2013-05-16
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VINTAGE MP PRESS OVER is the device name listed in this FDA 510(k) record. The listed applicant is Shofu Dental Corporation. It received FDA 510(k) clearance on 2013-05-16 under 510(k) number K122614. 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 VINTAGE MP PRESS OVER?

VINTAGE MP PRESS OVER is a medical device that received FDA 510(k) clearance on 2013-05-16. The listed applicant is Shofu Dental Corporation. The 510(k) number is K122614.

When did VINTAGE MP PRESS OVER receive FDA 510(k) clearance?

VINTAGE MP PRESS OVER received FDA 510(k) clearance on 2013-05-16, under 510(k) number K122614.

Who is the listed applicant for VINTAGE MP PRESS OVER?

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

What is the FDA product code for VINTAGE MP PRESS OVER?

The FDA product code for VINTAGE MP PRESS OVER 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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