Medical Device Manufacturer · US , Secaucus , NJ

Noritake Co., Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1989

Recent clearances: ZIRPRIME, SUPER PORCELAIN EX-3 UNIVERSAL OPAQUE, SUPER PORCELAIN EX-3 PRESS

14

Total

14

Cleared

0

Denied

FDA 510(k) Regulatory Record - Noritake Co., Inc. Dental ✕

14 devices

1-14 of 14

Cleared Aug 12, 2011

Cleared Jun 30, 2011

SUPER PORCELAIN EX-3 UNIVERSAL OPAQUE

Cleared Nov 23, 2005

SUPER PORCELAIN EX-3 PRESS

Cleared May 11, 2005

CZR PRESS LF STAINS

Cleared Feb 07, 2005

KATANA ZIRCONIA

Cleared Jan 11, 2005

Cleared Dec 22, 2003

Cleared Oct 24, 2003

Cleared Sep 03, 1999

Cleared Aug 27, 1999

SUPER PORCELAIN TI-22

Cleared Dec 22, 1998

SUPER PORCELAIN STAIN- PURE WHITE

Cleared Nov 03, 1998

SUPER PORCELAIN ADDMATE

Cleared Oct 30, 1998

PASTE OPAQUE EX-3

Cleared Jan 10, 1989

NORITAKE SUPER PORCELAIN EX-3