Sybron Dental Specialties, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sybron Dental Specialties, Inc. - FDA 510(k) Cleared Devices
106
Total
106
Cleared
0
Denied
Sybron Dental Specialties, Inc. has 106 FDA 510(k) cleared dental devices. Based in Glendora, US.
Historical record: 106 cleared submissions from 1994 to 2010.
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 - Sybron Dental Specialties, Inc.
106 devices
Cleared
Apr 05, 2010
CENTURY MODEL 105C
Dental
164d
Cleared
Oct 14, 2009
SONICFILL 2010
Dental
181d
Cleared
Sep 04, 2008
SONICFLEX 2003 AND SONICFLEX LUX 2003 L WITH INSTRUMENT TIPS
Dental
234d
Cleared
Sep 03, 2008
SUPERTORQUE HIGH-SPEED HANDPIECES AND GENTLEPOWER HANDPIECES AND ATTACHEMENTS
Dental
267d
Cleared
Sep 21, 2007
FIXAFLOSS
Dental
100d
Cleared
Jul 19, 2007
MODIFICATION TO KAVO QUATTROCARE
Dental
72d
Cleared
May 25, 2007
REMOVABLE ARYLIC HERBST, ALLESEE SNORE APPLIANCE (ASA), AND ENOCH SNORINATOR
Dental
109d
Cleared
Mar 28, 2006
OPTIBOND ALL-IN-ONE
Dental
33d
Cleared
Feb 03, 2006
TEMPBOND CLEAR WITH TRICLOSAN
Dental
43d
Cleared
Jan 03, 2006
EXPASYL POWER APPLICATOR
Dental
174d
Cleared
Apr 15, 2005
KERR VPS IMPRESSION MATERIAL
Dental
37d
Cleared
Nov 15, 2004
D3 CHROMA
Dental
69d
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