Medical Device Manufacturer · US , Ardmore , OK

Imtec Corp. - FDA 510(k) Cleared Devices

28 submissions · 28 cleared · Since 1991

28

Total

28

Cleared

0

Denied

FDA 510(k) Regulatory Record - Imtec Corp. Dental ✕

24 devices

1-24 of 24

Cleared Sep 19, 2008

MDI MII ONE-PIECE IMPLANT, 2.9MM

Cleared Dec 12, 2007

ENDURE IMPLANT, MODEL 5108, 5111, 5113, 5114

Cleared Jan 13, 2005

ENDURE IMPLANT, MODELS 3508, 4308, 3520, 4320

Cleared Sep 15, 2004

Cleared Jan 15, 2004

LEXATITE QUICK ACRYLIC

Cleared Aug 12, 2003

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

Cleared Apr 23, 2003

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

Cleared Feb 21, 2003

SABER TECH IMPLANTS SYSTEM

Cleared Dec 03, 2002

IMTEC SENDAX MDI ORTHO6 AND ORTHO8

Cleared Jul 19, 2002

Cleared Jun 14, 2002

SECURE RELINE/PICKUP MATERIAL

Cleared Apr 10, 2002

BIOCELLECT -PERIO

Cleared Jun 12, 2001

Cleared Jun 21, 1999

Cleared Apr 13, 1999

MODIFICATION TO IMTEC SENDAX MDI

Cleared Mar 03, 1998

IMTEC/BIOBARRIER MEMBRANE

Cleared Nov 19, 1997

IMTEC BONE COLLECTOR SYSTEM

Cleared Nov 18, 1997

Cleared Aug 26, 1997

IMTEC BIOBARRIER MEMBRANE

Cleared Apr 30, 1997

IMTEC/TITANIUM MESH

Cleared Feb 06, 1996

IMTEC BIOBARRIER

Cleared Aug 24, 1994

HEXLOCK/HEXLOCK SCREW

Cleared Jan 12, 1993

Cleared Dec 10, 1991