Clinical Safety and Efficacy of the VDyne Transcatheter Tricuspid Valve Replacement System for the Treatment of Tricuspid Regurgitation ( VISTA-US)

The purpose of this clinical study is to evaluate the safety and clinical efficacy of the VDyne System in the treatment of symptomatic severe tricuspid regurgitation (TR).

Inclusion Criteria: * Symptomatic severe tricuspid valve regurgitation of primary or secondary etiology. * NYHA class ≥ II. If NYHA Class IV, patient must be ambulatory. * Subject is adequately treated with medical therapy for heart failure ≥ 30 days prior to * index procedure, including a diuretic. * Heart Team determines patient is a recommended candidate for the VDyne System. * Age \>18 years at time of index procedure. * Clinical Screening Committee (CSC) and Imaging Core Labs confirm suitability for treatment with the VDyne System. Exclusion Criteria: * Patient anatomy (cardiac and vascular) is not suitable for VDyne System as assessed by Imaging Core Labs, Sponsor or Clinical Screening Committee (CSC) * Intolerance to procedural anticoagulation or post-procedural antiplatelet/ anticoagulation regimen that cannot be medically managed * Hypersensitivity to nickel or titanium * Left Ventricular Ejection Fraction (LVEF) \70 mmHg. * History or rheumatic fever * Significant coronary artery disease requiring treatment such as symptomatic, unresolved multi-vessel or unprotected left main coronary artery disease. * Any planned surgery or interventional procedure within 30 days prior to or 30 days following the implant procedure. This includes any planned concomitant cardiovascular procedure such as CABG, PCI, pulmonary vein ablation, left atrial appendage occlusion, septal defect repair, etc. * Unresolved severe symptomatic carotid stenosis (\> 70% by ultrasound). * Cardiac resynchronization therapy device or implantable pulse generator implanted within 60 days of planned implant procedure. * Permanent pacing leads that will interfere with delivery or implantation of the VDyne Valve. * Cardiogenic shock or hemodynamic instability requiring inotropes or mechanical support devices at the time of planned implant procedure. * Prior tricuspid valve surgery or catheter-based therapy with permanent residual device(s) implanted that would preclude delivery or implantation of the VDyne Valve (e.g. valve replacement, edge to edge repair, etc.). * Significant valvular heart disease requiring intervention other than the tricuspid valve. * Known significant intracardiac shunt (e.g. septal defect) * Cerebrovascular accident (stroke, TIA) within 6 months of treatment procedure. * Severe lung disease (severe COPD or continuous use of home oxygen or oral steroids). * Acute myocardial infarction (AMI) within 30 days. * Significant renal dysfunction (eGFR\ 11 / CHILD class C). * Bleeding requiring transfusion within prior 30 days. * Coagulopathy or other clotting disorder that cannot be medically managed. * Chronic immunosuppression or other condition that could impair healing response. * Any of the following: leukopenia, chronic anemia (Hgb \< 9), thrombocytopenia, history of bleeding diathesis, or coagulopathy. * Unwilling to receive blood products. * Known hypersensitivity or contraindication to procedural or post-procedural medications (e.g., contrast solution) which cannot be adequately managed medically. * Life expectancy less than 12 months due to non-cardiac comorbidities. * Treatment is not expected to provide benefit (futile). * Current IV Drug user (must be free drug abuse for \> 1 year). * Pregnant, lactating or planning pregnancy within next 12 months. * Vulnerable patient groups (minors, cognitively impaired persons, prisoners, persons whose willingness to volunteer could be unduly influenced by the expectation of benefits associated with participation or of retaliatory response from senior members of a hierarchy in case of refusal to participate, such as students, residents, and employees). * Currently participating in an investigational drug or device trial that has not reached its primary endpoint or is likely to interfere with this study. * Patient (or legal guardian) unable or unwilling to provide written, informed consent before study enrollment. * Patient unable or unwilling to comply with study required testing and follow-up visits