Kuraray Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kuraray Medical, Inc. - FDA 510(k) Cleared Devices
42
Total
42
Cleared
0
Denied
Kuraray Medical, Inc. has 42 FDA 510(k) cleared dental devices. Based in New York, US.
Historical record: 42 cleared submissions from 2001 to 2012.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kuraray Medical, Inc.
42 devices
Cleared
Mar 30, 2012
PANAVIA SA CEMENT HANDMIX VALUE PACK (UNIVERSAL (A2), WHITE) PANAVIA SA...
Dental
52d
Cleared
Mar 30, 2012
PANAVIA SA CEMENT AUTOMIX VALUE PACK (UNIVERSAL (A2), WHITE) PANAVIA SA...
Dental
52d
Cleared
Oct 14, 2011
CLEARFIL TRI-S BOND PLUS SINGLE DOSE STANDARD / VALUE / INTRODUCTORY PACK
Dental
94d
Cleared
Mar 05, 2010
CLEARFIL MAJETY POSTERIOR
Dental
29d
Cleared
Oct 27, 2009
CLEARFIL MAJESTY POSTERIOR PLT
Dental
90d
Cleared
Jul 28, 2008
CLEARFIL SA CEMENT
Dental
53d
Cleared
Jun 20, 2007
CLEARFIL MAJESTY POSTERIOR PLT
Dental
54d
Cleared
Mar 21, 2007
CLEARFIL MAJESTY ESTHETIC PLT
Dental
44d
Cleared
Nov 08, 2006
K-ETCHANT GEL
Dental
83d
Cleared
Sep 28, 2006
CLEARFIL CERAMIC PRIMER
Dental
85d
Cleared
Sep 27, 2006
CLEARFIL DC BOND
Dental
43d
Cleared
Sep 26, 2006
CLEARFIL ESTHETIC CEMENT & DC BOND
Dental
40d
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