Kensey Nash Corp.
Kensey Nash Corp. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2011.
Top product codes for Kensey Nash Corp.
Recent clearances by Kensey Nash Corp.
- K103787 — MEDEOR MATRIX
- K091192 — KENSEY NASH P1076 COLLAGEN DENTAL MEMBRANE, MODEL 20655-XX
- K091499 — MEDEOR MATRIX, MODELS 30010-XX (HYDRATED); 30020-XX (DRY)
- K090919 — KENSEY NASH FIBRILLAR COLLAGEN DENTAL MEMBRANE
- K073519 — QUICKCAT EXTRACTION CATHETER, MODEL 60090-01
- K071695 — KENSEY NASH MACROPORE SHIELD
- K072384 — MODIFICATION TO COPIOS BONE VOID FILLER SPONGE & PASTE
- K072195 — THROMCAT THROMBECTOMY CATHETER SYSTEM
- K071237 — COPIOS BONE VOID FILLER SPONGE AND PASTE
- K062870 — TRIACTIV FX EMBOLIC PROTECTION SYSTEM, MODEL PN 60040-02; -03
- K061772 — TRIACTIV FX EMBOLIC PROTECTION SYSTEM
- K060016 — THROMCAT THROMBECTOMY CATHETER SYSTEM
- K060092 — QUICKCAT EXTRACTION CATHETER
- K043259 — BIOBLANKET SURGICAL MESH
- K042040 — TRIACTIV SYSTEM
- K041923 — BIOBLANKET
- K011943 — IMPRO VISE ABSORBABLE CEMENT FLOW RESTRICTOR
- K926089 — KENSEY NASH WUIK-SERT(TM) ENDOSCOPIC SURG GRASPER
- K923726 — KENSEY NASH DYNAMIC CLIP SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.