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Kensey Nash Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K103787MEDEOR MATRIXFebruary 7, 2011
K091192KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XXNovember 2, 2009
K091499MEDEOR MATRIX, MODELS 30010-XX (HYDRATED); 30020-XX (DRY)October 22, 2009
K090919KENSEY NASH FIBRILLAR COLLAGEN DENTAL MEMBRANEOctober 2, 2009
K073519QUICKCAT EXTRACTION CATHETER, MODEL 60090-01March 28, 2008
K071695KENSEY NASH MACROPORE SHIELDDecember 31, 2007
K072384MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTESeptember 21, 2007
K072195THROMCAT THROMBECTOMY CATHETER SYSTEMAugust 23, 2007
K071237COPIOS BONE VOID FILLER SPONGE AND PASTEJune 1, 2007
K062870TRIACTIV FX EMBOLIC PROTECTION SYSTEM, MODEL PN 60040-02; -03October 20, 2006
K061772TRIACTIV FX EMBOLIC PROTECTION SYSTEMJuly 11, 2006
K060016THROMCAT THROMBECTOMY CATHETER SYSTEMApril 25, 2006
K060092QUICKCAT EXTRACTION CATHETERMarch 9, 2006
K043259BIOBLANKET SURGICAL MESHAugust 15, 2005
K042040TRIACTIV SYSTEMMarch 23, 2005
K041923BIOBLANKETSeptember 8, 2004
K011943IMPRO VISE ABSORBABLE CEMENT FLOW RESTRICTORSeptember 19, 2001
K926089KENSEY NASH WUIK-SERT(TM) ENDOSCOPIC SURG GRASPERJuly 23, 1993
K923726KENSEY NASH DYNAMIC CLIP SYSTEMApril 6, 1993