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FDA 510(k)

VMK 68 AND VMK 68N DENTAL PORCELAIN KIT

K-Number: K901862 · 1990-10-10

ApplicantVident
Decision Date1990-10-10
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VMK 68 AND VMK 68N DENTAL PORCELAIN KIT is the device name listed in this FDA 510(k) record. The listed applicant is Vident. It received FDA 510(k) clearance on 1990-10-10 under 510(k) number K901862. 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 VMK 68 AND VMK 68N DENTAL PORCELAIN KIT?

VMK 68 AND VMK 68N DENTAL PORCELAIN KIT is a medical device that received FDA 510(k) clearance on 1990-10-10. The listed applicant is Vident. The 510(k) number is K901862.

When did VMK 68 AND VMK 68N DENTAL PORCELAIN KIT receive FDA 510(k) clearance?

VMK 68 AND VMK 68N DENTAL PORCELAIN KIT received FDA 510(k) clearance on 1990-10-10, under 510(k) number K901862.

Who is the listed applicant for VMK 68 AND VMK 68N DENTAL PORCELAIN KIT?

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

What is the FDA product code for VMK 68 AND VMK 68N DENTAL PORCELAIN KIT?

The FDA product code for VMK 68 AND VMK 68N DENTAL PORCELAIN KIT is EIH.

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Other records listing Vident 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.

K063768TITANIUM SCALLOPED ABUTMENTK060441VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9, MODEL NX98K052710VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9,K052130VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40K050362VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)K022996VITA IN-CERAM YZ CUBES FOR CEREC

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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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