WATCHMAN FLX device on white background with FDA approved orange badge.

WATCHMAN FLXTM Pro

Left Atrial Appendage Closure Device

featuring HEMOCOAT™ Technology

Now FDA approved - WATCHMAN FLX™ Pro Device

Built on the proven safety profile of the WATCHMAN FLX Device, the WATCHMAN FLX Pro Device is designed to enhance the healing process and optimize the therapy for more patients.

WATCHMAN FLX Pro pre-clinical data

The fluoropolymer-coated WATCHMAN FLX Pro device showed significantly less thrombus and reduced inflammation in a challenging canine model. Mechanistic studies demonstrated that the WATCHMAN FLX Pro device binds more albumin, leading to reduced platelet activation, less inflammation, and greater endothelial coverage (EC).1

WATCHMAN™ TruPlan™ CT Imaging Software

WATCHMAN TruPlan CT Imaging Software is purpose-built to facilitate patient screening and procedure planning for LAAC. WATCHMAN TruPlan Software offers a full feature set that allows you to visualize each unique anatomy and to create a customized procedure plan for your LAAC implants.

WATCHMAN TruSteer™ Access System

Designed to improve implant success, the WATCHMAN TruSteer™ Access System optimizes coaxial device positioning in the widest range of LAA anatomies.

Learn more about WATCHMAN Integrated LAAC Solutions

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WATCHMAN™ TruPlan™ is developed and owned by Circle Cardiovascular Imaging Inc. (Calgary, AB, Canada), and Boston Scientific is the exclusive reseller of WATCHMAN TruPlan.

Sources:

  1. Saliba et al. JACC: Clinical Electrophysiology, May 2023. Bench testing or pre-clinical study results may not necessarily be indicative of clinical performance. N=12 in a pre-clinical canine study.