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FDA 510(k)

VINTAGE ART

K-Number: K080834 · 2008-06-11

ApplicantShofu Dental Corp.
Decision Date2008-06-11
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VINTAGE ART 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 2008-06-11 under 510(k) number K080834. 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 ART?

VINTAGE ART is a medical device that received FDA 510(k) clearance on 2008-06-11. The listed applicant is Shofu Dental Corp.. The 510(k) number is K080834.

When did VINTAGE ART receive FDA 510(k) clearance?

VINTAGE ART received FDA 510(k) clearance on 2008-06-11, under 510(k) number K080834.

Who is the listed applicant for VINTAGE ART?

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 ART?

The FDA product code for VINTAGE ART 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 RESIGLASSK110235BEAUTIBOND MULTIK110252BEAUTIBOND MULTI PR PLUSK101621LITE ARTK101603BEAUTIFIL FLOW PLUSK093559VINTAGE 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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