Dentsply Interntional is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dentsply Interntional - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Dentsply Interntional has 13 FDA 510(k) cleared dental devices. Based in York, US.
Historical record: 13 cleared submissions from 2007 to 2009.
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 - Dentsply Interntional
13 devices
Cleared
Dec 02, 2009
X-SMART EASY
Dental
98d
Cleared
Jul 24, 2009
ELATION MB METAL REINFORCED PLASTIC BRACKET
Dental
18d
Cleared
Mar 20, 2009
ALLURE MB CERAMIC BRACKETS
Dental
25d
Cleared
Jan 29, 2009
STER-MATE STERILE LAVAGE KIT
Dental
115d
Cleared
Nov 07, 2008
MYSTIQUE MB CERAMIC BRACKETS
Dental
32d
Cleared
May 22, 2008
PRE-CEMENTED ORTHODONTIC BRACKET SYSTEM EXTENSION
Dental
15d
Cleared
Apr 18, 2008
MODIFIED TEMPRX ESTHETIC PROVISIONAL SYSTEM
Dental
72d
Cleared
Apr 11, 2008
COMPOSITE ALIGNER BUTTON
Dental
71d
Cleared
Mar 26, 2008
MTA ROOT CANAL SEALER
Dental
58d
Cleared
Jan 23, 2008
SELF-ADHESIVE RESIN CEMENT
Dental
71d
Cleared
Jan 07, 2008
MTA ADVANCED MATERIAL
Dental
53d
Cleared
Sep 04, 2007
OSTEOGRAF/N-300
Dental
63d
Cleared
Aug 03, 2007
MODIFICATION TO: OSTEOGRAF/N-700
Dental
8d