Medical Device Manufacturer · US , Secaucus , NJ

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

14 submissions · 14 cleared · Since 1989

Total

Cleared

Denied

Noritake Co., Inc. has 14 FDA 510(k) cleared dental devices. Based in Secaucus, US.

Historical record: 14 cleared submissions from 1989 to 2011.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Noritake Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

14 devices

1-12 of 14

SUPER PORCELAIN EX-3 UNIVERSAL OPAQUE

K111107 · EIH

Dental · 71d

Cleared Nov 23, 2005

SUPER PORCELAIN EX-3 PRESS

SUPER PORCELAIN TI-22

K992024 · EIH

Dental · 72d

Cleared Dec 22, 1998

SUPER PORCELAIN STAIN- PURE WHITE

K983470 · EIH

Dental · 82d

Cleared Nov 03, 1998

SUPER PORCELAIN ADDMATE

K983247 · EIH

Dental · 48d

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

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

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