Kensey Nash Corp. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Kensey Nash Corp. has 19 FDA 510(k) cleared medical devices. Based in Exton, US.
Historical record: 19 cleared submissions from 1993 to 2011.
Browse the FDA 510(k) cleared devices submitted by Kensey Nash Corp. Filter by specialty or product code using the sidebar.
19 devices
Cleared
Feb 07, 2011
MEDEOR MATRIX
General & Plastic Surgery
42d
Cleared
Nov 02, 2009
KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX
Dental
193d
Cleared
Oct 22, 2009
MEDEOR MATRIX, MODELS 30010-XX (HYDRATED)
General & Plastic Surgery
154d
Cleared
Oct 02, 2009
KENSEY NASH FIBRILLAR COLLAGEN DENTAL MEMBRANE
Dental
184d
Cleared
Mar 28, 2008
QUICKCAT EXTRACTION CATHETER, MODEL 60090-01
Cardiovascular
105d
Cleared
Dec 31, 2007
KENSEY NASH MACROPORE SHIELD
General & Plastic Surgery
194d
Cleared
Sep 21, 2007
MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTE
Orthopedic
28d
Cleared
Aug 23, 2007
THROMCAT THROMBECTOMY CATHETER SYSTEM
Cardiovascular
16d
Cleared
Jun 01, 2007
COPIOS BONE VOID FILLER SPONGE AND PASTE
Orthopedic
29d
Cleared
Oct 20, 2006
TRIACTIV FX EMBOLIC PROTECTION SYSTEM, MODEL PN 60040-02
Cardiovascular
25d
Cleared
Jul 11, 2006
TRIACTIV FX EMBOLIC PROTECTION SYSTEM
Cardiovascular
18d
Cleared
Apr 25, 2006
THROMCAT THROMBECTOMY CATHETER SYSTEM
Cardiovascular
112d