FDA 510(k) Applications Submitted by IMTEC CORP.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K021437 |
05/06/2002 |
SECURE SOFT |
IMTEC CORP. |
| K021586 |
05/14/2002 |
SECURE RELINE/PICKUP MATERIAL |
IMTEC CORP. |
| K081347 |
05/14/2008 |
ILUMA VISION |
IMTEC CORP. |
| K023067 |
09/16/2002 |
IMTEC SENDAX MDI ORTHO6 AND ORTHO8 |
IMTEC CORP. |
| K033432 |
10/28/2003 |
LEXATITE QUICK ACRYLIC |
IMTEC CORP. |
| K950306 |
01/25/1995 |
IMTEC BIOBARRIER |
IMTEC CORP. |
| K081653 |
06/12/2008 |
MDI MII ONE-PIECE IMPLANT, 2.9MM |
IMTEC CORP. |
| K024044 |
12/06/2002 |
SABER TECH IMPLANTS SYSTEM |
IMTEC CORP. |
| K031106 |
04/08/2003 |
IMTEC SENDAX MDI AND MDI PLUS ENDOSSEOUS IMPLANT, MODELS OB-XX, SH-XX, MOB-22, MSH-XX |
IMTEC CORP. |
| K042289 |
08/24/2004 |
MDI ORTHO |
IMTEC CORP. |
| K072660 |
09/21/2007 |
ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114 |
IMTEC CORP. |
| K053046 |
10/28/2005 |
ILUMA ORTHOCAT/DENTALCAT |
IMTEC CORP. |
| K043226 |
11/22/2004 |
ENDURE IMPLANT, MODELS 3508, 4308, 3520, 4320 |
IMTEC CORP. |
| K030243 |
01/23/2003 |
ENDURE IMPLANT, MODEL 3508,3511,3514,4308,4311,4314 |
IMTEC CORP. |
| K973180 |
08/25/1997 |
IMTEC BONE TAC |
IMTEC CORP. |
| K974752 |
12/19/1997 |
IMTEC/BIOBARRIER MEMBRANE |
IMTEC CORP. |
| K020396 |
02/06/2002 |
BIOCELLECT -PERIO |
IMTEC CORP. |
| K970841 |
03/07/1997 |
IMTEC/TITANIUM MESH |
IMTEC CORP. |
| K010775 |
03/14/2001 |
BIOCELLECT |
IMTEC CORP. |
| K990983 |
03/24/1999 |
MODIFICATION TO IMTEC SENDAX MDI |
IMTEC CORP. |
| K972240 |
06/16/1997 |
IMTEC BIOBARRIER MEMBRANE |
IMTEC CORP. |
| K982951 |
08/24/1998 |
IMTEC BIOPIN |
IMTEC CORP. |
| K973248 |
08/29/1997 |
IMTEC BONE COLLECTOR SYSTEM |
IMTEC CORP. |
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