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FDA 510(k)

SUPER PORCELAIN TI-22

K-Number: K992024 · 1999-08-27

ApplicantNoritake Co., Inc.
Decision Date1999-08-27
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SUPER PORCELAIN TI-22 is the device name listed in this FDA 510(k) record. The listed applicant is Noritake Co., Inc.. It received FDA 510(k) clearance on 1999-08-27 under 510(k) number K992024. 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 SUPER PORCELAIN TI-22?

SUPER PORCELAIN TI-22 is a medical device that received FDA 510(k) clearance on 1999-08-27. The listed applicant is Noritake Co., Inc.. The 510(k) number is K992024.

When did SUPER PORCELAIN TI-22 receive FDA 510(k) clearance?

SUPER PORCELAIN TI-22 received FDA 510(k) clearance on 1999-08-27, under 510(k) number K992024.

Who is the listed applicant for SUPER PORCELAIN TI-22?

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

What is the FDA product code for SUPER PORCELAIN TI-22?

The FDA product code for SUPER PORCELAIN TI-22 is EIH.

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Other records listing Noritake Co., Inc. 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.

K111383ZIRPRIMEK111107SUPER PORCELAIN EX-3 UNIVERSAL OPAQUEK052304SUPER PORCELAIN EX-3 PRESSK050920CZR PRESS LF STAINSK050160KATANA ZIRCONIAK043462CZR PRESS LF

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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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