Dentsply Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dentsply Intl., Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Dentsply Intl., Inc. has 12 FDA 510(k) cleared dental devices. Based in York, US.
Historical record: 12 cleared submissions from 2005 to 2014.
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 Intl., Inc.
12 devices
Cleared
Aug 20, 2014
ANKYLOS C/X IMPLANT SYSTEM
Dental
190d
Cleared
Jul 23, 2013
CAVITRON PROPHY-JET AIR POLISHING PROPHYLAXIS SYSTEM
Dental
117d
Cleared
Feb 14, 2011
QMIX 2IN1 ENDODONTIC IRRIGATING SOLUTION
Dental
104d
Cleared
Oct 30, 2009
PRE-CEMENTED ORTHODONTIC BRACKET SYSTEM EXTENSION II
Dental
17d
Cleared
May 22, 2009
ANKYLOS C/X DENTAL IMPLANT SYSTEM
Dental
151d
Cleared
Oct 29, 2008
DURASHIELD PLUS
Dental
86d
Cleared
Jan 28, 2008
AXIS SYSTEM
Dental
97d
Cleared
Dec 19, 2007
DENTIN DESENSITIZER AGENT
Dental
44d
Cleared
Nov 27, 2006
MOUTHGUARD AND ALIGNER MATERIALS
Dental
68d
Cleared
Oct 27, 2006
VISTADENT OC - VERSION 4
Radiology
213d
Cleared
Dec 08, 2005
BIOPURE MTAD ROOT CANAL CLEANSER
Dental
24d
Cleared
Nov 22, 2005
VISTADENT AT COMPLETE, MODEL 3.1
Radiology
27d