Medical Device Manufacturer · US , Ardmore , OK

Imtec Corp. - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 1991

Recent clearances: MDI MII ONE-PIECE IMPLANT, 2.9MM, ILUMA VISION, ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114

Total

Cleared

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.

510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.

Imtec Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Imtec Corp.

28 devices

1-12 of 28

Cleared Sep 19, 2008

MDI MII ONE-PIECE IMPLANT, 2.9MM

ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114

K072660 · DZE

Dental · 82d

Cleared Nov 08, 2005

ILUMA ORTHOCAT/DENTALCAT

K053046 · JAK

Radiology · 11d

Cleared Jan 13, 2005

ENDURE IMPLANT, MODELS 3508, 4308, 3520, 4320

LEXATITE QUICK ACRYLIC

K033432 · EBG

Dental · 79d

Cleared Aug 12, 2003

IMTEC SENDAX MDI AND MDI PLUS ENDOSSEOUS IMPLANT, MODELS OB-XX, SH-XX,...

K031106 · DZE

Dental · 126d

Cleared Apr 23, 2003

ENDURE IMPLANT, MODEL 3508,3511,3514,4308,4311,4314

K030243 · DZE

Dental · 90d

Cleared Feb 21, 2003

SABER TECH IMPLANTS SYSTEM

K024044 · DZE

Dental · 77d

Cleared Dec 03, 2002

IMTEC SENDAX MDI ORTHO6 AND ORTHO8

Imtec Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Imtec Corp.

Filters