Teknimed S A

FDA Filings

This page includes the latest FDA filings for Teknimed S A. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Owner/Operator Registration

FDA Filings

Device Company	Device	Date
PMN K103433 TEKNIMED SA	F20	2011-01-03
PMN K090435 TEKNIMED SA	VERTECEM	2009-12-21
PMN K083005 TEKNIMED SA	NANGEL	2009-03-04
PMN K080873 TEKNIMED SA	OPACITY + BONE CEMENT	2008-08-28
PMN K062102 TEKNIMED SA	ODONCER	2007-04-16
PMN K043593 TEKNIMED SA	SPINE-FIX BIOMIMETIC BONE CEMENT	2006-03-17
PMN K042911 TEKNIMED SA	CEMENTEK LV	2004-12-27
PMN K041493 TEKNIMED SA	CEMENTEK	2004-08-19
PMN K040669 TEKNIMED SA	CERAFORM BONE VOID FILLER	2004-05-03
PMN K031826 TEKNIMED SA	TRIHA +	2003-11-28
PMN K032685 TEKNIMED SA	CEMSTOP CEMENT RESTRICTOR	2003-11-26

Similar & Related FDA Registered Companies

• TEKNIMED SAS