Medical Device Manufacturer · US , New York , NY

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

11 submissions · 11 cleared · Since 1997

11

Total

11

Cleared

0

Denied

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

11 devices

1-11 of 11

Cleared Nov 17, 2011

CLEARFIL DC CORE PLUS

Cleared Oct 14, 2011

CLEARFIL TRI-S BOND PLUS

Cleared Feb 09, 2007

CLEARFIL MAJESTY POSTERIOR

Cleared Feb 02, 2007

CLEARFIL MAJESTY FLOW

Cleared Dec 08, 2006

Cleared Sep 18, 2000

MODIFICATION TO PANAVIA F

Cleared Nov 13, 1998

Cleared Sep 22, 1998

CHROMA ZONE COLOR STAIN

Cleared Aug 10, 1998

Cleared Jan 29, 1998

CLEARFIL LINER BOND 2V

Cleared Dec 17, 1997