Imtec Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Imtec Corp. - FDA 510(k) Cleared Devices
28
Total
28
Cleared
0
Denied
Imtec Corp. has 28 FDA 510(k) cleared dental devices. Based in Ardmore, US.
Historical record: 28 cleared submissions from 1991 to 2008.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Imtec Corp.
28 devices
Cleared
Sep 19, 2008
MDI MII ONE-PIECE IMPLANT, 2.9MM
Dental
99d
Cleared
May 28, 2008
ILUMA VISION
Radiology
14d
Cleared
Dec 12, 2007
ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114
Dental
82d
Cleared
Nov 08, 2005
ILUMA ORTHOCAT/DENTALCAT
Radiology
11d
Cleared
Jan 13, 2005
ENDURE IMPLANT, MODELS 3508, 4308, 3520, 4320
Dental
52d
Cleared
Sep 15, 2004
MDI ORTHO
Dental
22d
Cleared
Jan 15, 2004
LEXATITE QUICK ACRYLIC
Dental
79d
Cleared
Aug 12, 2003
IMTEC SENDAX MDI AND MDI PLUS ENDOSSEOUS IMPLANT, MODELS OB-XX, SH-XX,...
Dental
126d
Cleared
Apr 23, 2003
ENDURE IMPLANT, MODEL 3508,3511,3514,4308,4311,4314
Dental
90d
Cleared
Feb 21, 2003
SABER TECH IMPLANTS SYSTEM
Dental
77d
Cleared
Dec 03, 2002
IMTEC SENDAX MDI ORTHO6 AND ORTHO8
Dental
78d
Cleared
Jul 19, 2002
SECURE SOFT
Dental
74d