ClearanceBrief
Company ยท US

Noritake Co., Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 2011. Name variants (Inc, Corp, punctuation) are merged.

14510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
EIHPowder, Porcelain14

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 12, 2011K111383ZIRPRIME
Noritake Co., Inc.
EIH
Jun 30, 2011K111107SUPER PORCELAIN EX-3 UNIVERSAL OPAQUE
Noritake Co., Inc.
EIH
Nov 23, 2005K052304SUPER PORCELAIN EX-3 PRESS
Noritake Co., Inc.
EIH
May 11, 2005K050920CZR PRESS LF STAINS
Noritake Co., Inc.
EIH
Feb 7, 2005K050160KATANA ZIRCONIA
Noritake Co., Inc.
EIH
Jan 11, 2005K043462CZR PRESS LF
Noritake Co., Inc.
EIH
Dec 22, 2003K031968CERABIEN ZR
Noritake Co., Inc.
EIH
Oct 24, 2003K033049CZR PRESS
Noritake Co., Inc.
EIH
Sep 3, 1999K992023GRAND CERAM
Noritake Co., Inc.
EIH
Aug 27, 1999K992024SUPER PORCELAIN TI-22
Noritake Co., Inc.
EIH
Dec 22, 1998K983470SUPER PORCELAIN STAIN- PURE WHITE
Noritake Co., Inc.
EIH
Nov 3, 1998K983247SUPER PORCELAIN ADDMATE
Noritake Co., Inc.
EIH
Oct 30, 1998K982766PASTE OPAQUE EX-3
Noritake Co., Inc.
EIH
Jan 10, 1989K884356NORITAKE SUPER PORCELAIN EX-3
Noritake Co., Inc.
EIH

Latest recalls

DateFirm and productCodeLinked 510(k)
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