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FDA 510(k)

VISION PORCELAIN

K-Number: K990790 · 1999-04-02

ApplicantServo Dental USA, Inc.
Decision Date1999-04-02
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VISION PORCELAIN is the device name listed in this FDA 510(k) record. The listed applicant is Servo Dental USA, Inc.. It received FDA 510(k) clearance on 1999-04-02 under 510(k) number K990790. 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 VISION PORCELAIN?

VISION PORCELAIN is a medical device that received FDA 510(k) clearance on 1999-04-02. The listed applicant is Servo Dental USA, Inc.. The 510(k) number is K990790.

When did VISION PORCELAIN receive FDA 510(k) clearance?

VISION PORCELAIN received FDA 510(k) clearance on 1999-04-02, under 510(k) number K990790.

Who is the listed applicant for VISION PORCELAIN?

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

What is the FDA product code for VISION PORCELAIN?

The FDA product code for VISION PORCELAIN 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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