Sybron Dental Specialties is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sybron Dental Specialties - FDA 510(k) Cleared Devices
Recent clearances: Ormco Spark Aligner System
15
Total
15
Cleared
0
Denied
Sybron Dental Specialties has 15 FDA 510(k) cleared dental devices. Based in Newport Beach, US.
Historical record: 15 cleared submissions from 2006 to 2018.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Sybron Dental Specialties
15 devices
Cleared
Oct 11, 2018
Ormco Spark Aligner System
Dental
6d
Cleared
Apr 21, 2017
Steri-Cassette and Steri-Cage Sterilization Packaging System
General Hospital
269d
Cleared
Aug 05, 2016
Image Fast Set, Image Regular Set
Dental
199d
Cleared
Jul 27, 2016
Tubli-Seal, Tubli-Seal EWT,Tubli-Seal Xpress, Tubli-Seal EWT Xpress
Dental
279d
Cleared
May 06, 2016
Pulp Canal Sealer, Pulp Canal Sealer EWT
Dental
212d
Cleared
Apr 14, 2016
Sealapex tubes, Sealapex bulk package, Sealapex Xpress dual-barrel syringes
Dental
190d
Cleared
Sep 10, 2015
Zone, ZoneFree, Zone A1
Dental
94d
Cleared
Aug 17, 2015
Nexus Universal, Nexus Universal Chroma
Dental
90d
Cleared
Jun 19, 2015
Life Fast Set, Life Regular Set
Dental
105d
Cleared
Feb 05, 2015
SonicFill 2
Dental
87d
Cleared
May 30, 2013
TAKE 1 ADVANCE
Dental
62d
Cleared
Dec 11, 2008
HERCULITE ULTRA
Dental
87d
Cleared
Jan 19, 2007
LINGLOCK
Dental
280d
Cleared
Dec 05, 2006
DEMETRON A.2
Dental
54d
Cleared
Aug 03, 2006
VECTORS TEMPORARY ANCHORAGE SYSTEM
Dental
93d