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FDA 510(k)

VINTAGE PRESS, VINTAGE LF, VINTAGE LF STAIN

K-Number: K032416 · 2004-02-05

ApplicantShofu Dental Corp.
Decision Date2004-02-05
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VINTAGE PRESS, VINTAGE LF, VINTAGE LF STAIN is the device name listed in this FDA 510(k) record. The listed applicant is Shofu Dental Corp.. It received FDA 510(k) clearance on 2004-02-05 under 510(k) number K032416. 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 PRESS, VINTAGE LF, VINTAGE LF STAIN?

VINTAGE PRESS, VINTAGE LF, VINTAGE LF STAIN is a medical device that received FDA 510(k) clearance on 2004-02-05. The listed applicant is Shofu Dental Corp.. The 510(k) number is K032416.

When did VINTAGE PRESS, VINTAGE LF, VINTAGE LF STAIN receive FDA 510(k) clearance?

VINTAGE PRESS, VINTAGE LF, VINTAGE LF STAIN received FDA 510(k) clearance on 2004-02-05, under 510(k) number K032416.

Who is the listed applicant for VINTAGE PRESS, VINTAGE LF, VINTAGE LF STAIN?

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

What is the FDA product code for VINTAGE PRESS, VINTAGE LF, VINTAGE LF STAIN?

The FDA product code for VINTAGE PRESS, VINTAGE LF, VINTAGE LF STAIN is EIH.

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Other records listing Shofu Dental Corp. as applicant

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.

K111855HY-BOND RESIGLASSK110252BEAUTIBOND MULTI PR PLUSK110235BEAUTIBOND MULTIK101603BEAUTIFIL FLOW PLUSK101621LITE ARTK093559VINTAGE MP

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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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