Kensey Nash Corp.
FDA 510(k) medical device clearances.
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.