Danville Materials, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Danville Materials, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Danville Materials, Inc. has 11 FDA 510(k) cleared dental devices. Based in San Ramon, US.
Historical record: 11 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 - Danville Materials, Inc.
11 devices
Cleared
Sep 25, 2012
DMRC NANOFLOW DMRC NANOCOMPOSITE EBOND SURE ETCH GEL SURE ETCH LIQUID
Dental
89d
Cleared
Sep 21, 2011
Z BOND, PRELUDE ONE
Dental
82d
Cleared
May 27, 2011
SILJETR SYSTEM
Dental
81d
Cleared
Feb 04, 2011
TURBO TEMP 3
Dental
134d
Cleared
Dec 16, 2009
STARFILL 2B HV (HIGH VISCOSITY) ROCKCORE, MODEL: 90838 AND STARFILL 2B LV...
Dental
85d
Cleared
Sep 16, 2009
STAR VPS, MODEL 80014-01, FIRST QUATER, MODEL 90649, FIRST HALF, MODEL 89387
Dental
43d
Cleared
Mar 31, 2009
PRELUDE ONE
Dental
89d
Cleared
Jun 29, 2004
PRELUDE
Dental
78d
Cleared
Jan 09, 2004
PREPAIR
Dental
98d
Cleared
May 03, 2002
STARFLOW HV
Dental
57d
Cleared
Oct 10, 2001
SNOWPOST, SNOWLIGHT
Dental
77d