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Heraeus Kulzer,GmbH

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K083652	IBOND TOTAL ETCH	KLE	2009-01-21	View
510(k)	K080338	CUTTERSIL ACTIVATOR UNIVERSAL PLUS	ELW	2008-04-21	View
510(k)	K073554	NEUN	EBF	2008-02-04	View
510(k)	K062515	RETENTION FLOW OPAQUE	EBF	2006-11-22	View
510(k)	K050085	OSTEOPAL V	LOD	2005-09-14	View
510(k)	K050855	PALAMED G	LOD	2005-07-07	View
510(k)	K050854	PALACOS LV+G	LOD	2005-07-07	View
510(k)	K051006	IBOND NEXT GENERATION	KLE	2005-06-07	View
510(k)	K042199	TRANSLUX POWER BLUE	EBZ	2004-09-08	View
510(k)	K034049	HERADOR EC, PF, C, H, NH, G, GG AND MP; HERALOY U AND G; HERABOND N; ALBABOND C, B AND A; BIO HERANORM	EJT	2004-03-01	View

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