FDA 510(k) Applications Submitted by ITENA CLINICAL

FDA 510(k) Number Submission Date Device Name Applicant
K170207 01/24/2017 Obturys Itena Clinical
K162960 10/24/2016 TotalC-Ram ITENA CLINICAL
K121804 06/19/2012 PROVITEMP, DENTOTEMP, TOTALCEM, DENTOCEM ITENA CLINICAL
K121769 06/15/2012 DENTOCORE / DENTOCORE BODY ITENA CLINICAL
K122521 08/20/2012 PREVENT SEAL ITENA CLINICAL
K122522 08/20/2012 DENTOETCH QUICKBOND BOND ACTIVATOR ITENA CLINICAL
K122549 08/21/2012 DENTO TEMP ITENA CLINICAL
K122551 08/21/2012 PROVITEMP ITENA CLINICAL


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