Dentsply International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dentsply International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ATLANTIS ISUS Implant Suprastructures, Disposable Barrier Sleeves and Covers, ATLANTIS ISUS
36
Total
36
Cleared
0
Denied
Dentsply International, Inc. has 36 FDA 510(k) cleared dental devices. Based in York, US.
Historical record: 36 cleared submissions from 2006 to 2016.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Dentsply International, Inc.
36 devices
Cleared
Sep 21, 2016
ATLANTIS ISUS Implant Suprastructures
Dental
237d
Cleared
Jun 07, 2016
Disposable Barrier Sleeves and Covers
Dental
127d
Cleared
Feb 19, 2016
ATLANTIS ISUS
Dental
266d
Cleared
Jan 29, 2016
ATLANTIS Crown
Dental
172d
Cleared
Jan 14, 2016
ATLANTIS Abutment for NobelActive 3.0
Dental
269d
Cleared
Oct 30, 2015
Prime&Bond Elect Universal Dental Adhesive
Dental
136d
Cleared
Jun 16, 2015
Cavitron Touch Ultrasonic Scaling System
Dental
105d
Cleared
Feb 26, 2015
PROROOT MTA WHITE, PROROOT MTA GRAY
Dental
202d
Cleared
Jan 31, 2014
RAYPEX 6
Dental
219d
Cleared
Jan 22, 2014
ANKYLOS SYNCONE ABUTMENT 5(DEGREE)
Dental
231d
Cleared
Oct 11, 2013
MTM(R) CLEAR ALIGNER
Dental
92d
Cleared
Jul 05, 2013
ISUS IMPLANT SUPRASTRUCTURES
Dental
330d