| Symbol | BSX |
|---|---|
| Name | BOSTON SCIENTIFIC CORP |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | Surgical & Medical Instruments & Apparatus |
| Address | 300 BOSTON SCIENTIFIC WAY, MARLBOROUGH, MA 01752-1234 |
| Telephone | 508-683-4000 |
| Fax | — |
| — | |
| Website | https://www.bostonscientific.com |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | 0000885725 |
| Description | Boston Scientific produces less invasive medical devices that are inserted into the human body through small openings or cuts. It manufactures products for use in angioplasty, blood clot filtration, cardiac rhythm management, catheter-directed ultrasound imaging, structural heart disease, upper gastrointestinal tract diagnostics, interventional oncology, and treatment of incontinence. The firm markets its devices to healthcare professionals and institutions globally. Foreign sales account for nearly half of the firms total sales. Additional info from NASDAQ: |
(90% Positive) BOSTON SCIENTIFIC CORP (BSX) Announces Enrollment Update for innovation Due to Geopolitical Situation, Pandemic-Related Challenges, Patient Enrollment Issues, Regulatory Process, Manufacturing Considerations, Safety Review, Efficacy Assessment
Read moreBelo Sun Reports on New Court Proceedings Regarding the Volta Grande Gold Project
Read moreMonson Jonathan 🟡 adjusted position in 1.0K shares (1 derivative) of BOSTON SCIENTIFIC CORP (BSX) at $43.06 Transaction Date: Jul 01, 2026 | Filing ID: 006362
Read moreNew Form 11-K - BOSTON SCIENTIFIC CORP <b>Filed:</b> 2026-06-24 <b>AccNo:</b> 0000885725-26-000046 <b>Size:</b> 1 MB
Read moreDirector Mahoney Michael F 🔴 sold 386.8K shares of BOSTON SCIENTIFIC CORP (BSX) Transaction Date: May 28, 2026 | Filing ID: 005670
Read moreBelo Sun Announces 2026 Shareholder Meeting Voting Results and Corporate Update
Read more| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT00136929 | Senior PAMI: Primary Angioplasty Versus Thrombolytic Therapy for Acute Myocardi… | Na | Myocardial Infarction | Unknown | — | — | ClinicalTrials.gov |
| NCT00887055 | OPTIMA Bi-ventricular Capture Verification Study | — | Heart Failure | Withdrawn | — | — | ClinicalTrials.gov |
| NCT01227785 | Next Generation INCEPTA Implantable Cardioverter Defibrillator (ICD) and Cardia… | — | Sudden Cardiac Death | Completed | 2010-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01143220 | Japanese Assessment of Indication Based Programming | — | Heart Failure | Completed | 2010-08-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00920452 | The 4-SITE Field Following Study (4-SITE FF) | — | ICD and CRT-D Indicated Patients | Completed | 2009-05-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00800384 | Shockless Implant Evaluation | Na | Ventricular Fibrillation | Completed | 2009-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00833352 | Comparison of Right Ventricular Septal and Right Ventricular Apical Pacing in P… | Na | Systolic Heart Failure | Completed | 2008-11-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00711893 | Feature Assessment Study for Indications Based Programming | — | Ventricular Tachycardia | Completed | 2008-06-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00606710 | Cognis and Teligen 100 HE and Reliance Quadripolar Defibrillation Lead (4-Site)… | — | Ventricular Tachycardia, Ventricular Fibrillation | Completed | 2008-02-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00409604 | PROTECT : Pacing to Protect Heart for Damage From Blocked Heart Vessel and From… | Phase2 | Acute Myocardial Infarction | Completed | 2006-12-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00335036 | Pediatric Lead Extractability and Survival Evaluation (PLEASE) | Na | Ventricular Tachycardia | Terminated | 2006-06-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00305526 | REBEAT Resynchronisation and Beta-Blocker European Trial | Phase4 | Heart Failure | Terminated | 2006-04-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00848341 | Canadian Registry of ICD Implant Testing Procedures | — | Ventricular Fibrillation | Completed | 2006-01-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00257309 | Thrombolysis Versus Primary Angioplasty for AMI in Elderly Patients | Phase4 | Acute Myocardial Infarction | Terminated | 2005-04-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00180297 | Septal - Success Rate and Clinical Outcome of Septal Implant of Ventricular Def… | Na | Ventricular Tachycardia | Completed | 2005-04-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00848653 | ELECTION - The Electrode Configuration Cardiac Resynchronization Therapy (CRT) … | — | Heart Failure | Completed | 2004-11-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00180492 | Post-Approval Study of the Guidant Carotid Stent Systems and Embolic Protection… | Na | Atherosclerotic Disease, Carotid | Completed | 2004-10-01 | 2007-08-01 | ClinicalTrials.gov |
| NCT00180414 | MODULA Modul 7 VRR | Na | Atrial Fibrillation | Terminated | 2004-08-28 | 2008-05-07 | ClinicalTrials.gov |
| NCT00164190 | Routine Angioplasty and Stenting After Fibrinolysis for Acute Myocardial Infarc… | Na | Myocardial Infarction | Completed | 2004-07-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00180362 | Quick ICD Study: Is Extensive Electrophysiological Testing Before, During and A… | Phase4 | Cardiac Arrest | Completed | 2004-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00279175 | REPAIR-AMI: Intracoronary Progenitor Cells in Acute Myocardial Infarction (AMI) | Phase3 | Myocardial Infarction | Completed | 2004-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00116792 | PROVIDENCE:Prevention of Restenosis With Oral Rosiglitazone and the Vision Sten… | Phase2 | Coronary Artery Disease | Unknown | 2004-03-01 | — | ClinicalTrials.gov |
| NCT00180531 | Monitoring of Arrhythmias and HRV in Patients With Heart Failure Treated With t… | Phase4 | Congestive Heart Failure | Completed | 2004-02-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00180609 | SCANCAP Scandinavian Automatic Capture Study | — | Bradycardia | Completed | 2003-12-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00273091 | MODULA Modul 5 BEAT-HF | — | Heart Failure | Completed | 2003-08-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00192972 | A Randomized Trial of the Ostial Versus the Extra-Ostial Ablation Strategy for … | Na | Atrial Fibrillation | Completed | 2002-11-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00180440 | INSURE: INcidence Free SUrvival Before and After Implantable Cardioverter Defib… | — | Ventricular Fibrillation | Completed | 2002-07-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00180401 | MODULA-Study: Modul 10: Benefit of CRT-Therapy in CRT-Patients With QRS-Complex… | — | Heart Failure | Terminated | 2002-06-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00848835 | Long Term Integrity Follow-up Evaluation | — | Sudden Cardiac Death | Completed | 2002-03-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00180427 | VERRARI - "Are Ventricular Arrhythmic Episodes Reduced by Rate Response in ICDs… | Phase4 | Ventricular Fibrillation | Completed | 2001-06-01 | 2004-11-01 | ClinicalTrials.gov |
| NCT00180570 | SALT - Success of Active Versus Passive Lead Fixation of Atrial Pacing/Sensing … | Phase4 | Bradycardia | Suspended | 1997-01-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00475449 | The Stent or Surgery (SoS) Trial | Na | Coronary Artery Disease | Completed | 1996-11-01 | 2006-02-01 | ClinicalTrials.gov |
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| Contak Renewal (CRT-D) | Other | Phase PHASE4 | Heart Failure | TERMINATED | NCT00305526 |
| Renewal TR2 | Other | Phase PHASE4 | Congestive Heart Failure | COMPLETED | NCT00180531 |
| Renewal TR2 | Other | Phase PHASE4 | Congestive Heart Failure | COMPLETED | NCT00180531 |
| Percutaneous Coronary Intervention (PCI) | Other | Phase PHASE2 | Coronary Artery Disease | UNKNOWN | NCT00116792 |
| Percutaneous Coronary Intervention (PCI) | Other | Phase PHASE2 | Coronary Artery Disease | UNKNOWN | NCT00116792 |
| Routine Early Percutaneous Coronary Intervention after Thrombolysis | Other | Approved | Myocardial Infarction | COMPLETED | NCT00164190 |
| ICD | Other | Phase PHASE4 | Ventricular Fibrillation | COMPLETED | NCT00180427 |
| CRT device | Device | Preclinical | Heart Failure | COMPLETED | NCT00848653 |
| CRT device | Device | Preclinical | Heart Failure | COMPLETED | NCT00848653 |
| GUIDANT ICD SYSTEM | Other | Preclinical | Ventricular Fibrillation | COMPLETED | NCT00848341 |
| ICD | Other | Preclinical | Ventricular Fibrillation | COMPLETED | NCT00180440 |
| Automatic threshold test in Insignia Pacemakers from Guidant | Other | Preclinical | Bradycardia | COMPLETED | NCT00180609 |
| defibrillation lead (ENDOTAK EZ and RELIANCE) | Other | Preclinical | Sudden Cardiac Death | COMPLETED | NCT00848835 |
| defibrillation lead (ENDOTAK EZ and RELIANCE) | Other | Preclinical | Sudden Cardiac Death | COMPLETED | NCT00848835 |
| Temporary RV VVI pacing | Other | Phase PHASE2 | Acute Myocardial Infarction | COMPLETED | NCT00409604 |
| INCEPTA ICD or CRT-D | Other | Preclinical | Sudden Cardiac Death | COMPLETED | NCT01227785 |
| FineLine II Sterox, FineLine II Sterox, FineLine II Sterox EZ | Other | Phase PHASE4 | Bradycardia | SUSPENDED | NCT00180570 |
| FineLine II Sterox, FineLine II Sterox, FineLine II Sterox EZ | Other | Phase PHASE4 | Bradycardia | SUSPENDED | NCT00180570 |
| CRT device | Device | Preclinical | Heart Failure | WITHDRAWN | NCT00887055 |
| CRT device | Device | Preclinical | Heart Failure | WITHDRAWN | NCT00887055 |