FDA 510(k) Applications Submitted by GREG MOREAU
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K140144 |
01/22/2014 |
BENDA WEDGE |
CENTRIX, INC. |
| K060698 |
03/16/2006 |
CEMENT-IT ALL PURPOSE, MODEL N97 |
PENTRON CLINICAL TECHNOLOGIES |
| K971074 |
03/24/1997 |
THERAPAX SXT 150 |
PANTAK, INC. |
| K200764 |
03/24/2020 |
STATSTIX |
Centrix Incorporated |
| K060889 |
03/31/2006 |
SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SE |
PENTRON CLINICAL TECHNOLOGIES |
| K081887 |
07/02/2008 |
LUTE-IT II VENEER CEMENT, MODEL NO6 |
PENTRON CLINICAL TECHNOLOGIES |
| K052106 |
08/03/2005 |
SIMILE FLOW |
PENTRON CLINICAL TECHNOLOGIES |
| K052349 |
08/29/2005 |
AVANTE LED CURING UNIT, MODEL N44 |
PENTRON CLINICAL TECHNOLOGIES |
| K973315 |
09/03/1997 |
THERAPAX DXT 300 MODEL HF-300 |
PANTAK, INC. |
| K072545 |
09/10/2007 |
ARTISTE SE FLOWABLE COMPOSITE, MODEL N280 |
PENTRON CLINICAL TECHNOLOGIES |
| K152826 |
09/29/2015 |
NoCord |
CENTRIX, INC. |
| K072830 |
10/03/2007 |
RM BOND, MODEL J032 |
PENTRON CLINICAL TECHNOLOGIES |
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