Medical Device Manufacturer · US , New York , NY

Kuraray America, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1997

Recent clearances: CLEARFIL DC CORE PLUS, CLEARFIL TRI-S BOND PLUS, CLEARFIL MAJESTY POSTERIOR

View 11 510(k) Devices ↓

Total

Cleared

Denied

Kuraray America, Inc. has 11 FDA 510(k) cleared dental devices. Based in New York, US.

Historical record: 11 cleared submissions from 1997 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.

Kuraray America, Inc. is one of 20576 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kuraray America, Inc.

11 devices

1-11 of 11

Cleared Nov 17, 2011

CLEARFIL DC CORE PLUS

K111982 · EBF

Dental · 128d

Cleared Oct 14, 2011

CLEARFIL TRI-S BOND PLUS

K111980 · KLE

Dental · 94d

Cleared Feb 09, 2007

CLEARFIL MAJESTY POSTERIOR

K063595 · EBF

Dental · 67d

Cleared Feb 02, 2007

CLEARFIL MAJESTY FLOW

MODIFICATION TO PANAVIA F

CHROMA ZONE COLOR STAIN

CLEARFIL LINER BOND 2V

Kuraray America, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Kuraray America, Inc.

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