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EndoQuest Robotics Receives FDA IDE Approval for Flexible Robotic Colorectal Surgery System

8 months ago3 min read
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Key Insights

  • EndoQuest Robotics secured FDA approval for its Investigational Device Exemption (IDE) to initiate a pivotal clinical study of its Endoluminal Surgical (ELS) System.

  • The PARADIGM study will assess the safety and efficacy of the ELS system in robotic endoscopic submucosal dissection (ESD) for removing colorectal lesions across five U.S. sites.

  • Pre-clinical data suggests the ELS System offers superior outcomes, a shorter learning curve, and reduced procedure time compared to conventional techniques for colorectal lesion removal.

EndoQuest Robotics, a Houston-based medical device company, has received an Investigational Device Exemption (IDE) from the U.S. Food and Drug Administration (FDA) to commence a pivotal clinical trial for its innovative Endoluminal Surgical (ELS) System. This flexible robotic system is designed to improve the treatment of colorectal diseases through minimally invasive procedures.

PARADIGM Study Details

The IDE approval allows EndoQuest to begin the Prospective Assessment of a Robotic-Assisted Device in Gastrointestinal Medicine (PARADIGM) study. This multi-center, open-label study will enroll 50 subjects across five leading U.S. healthcare facilities: Brigham and Women’s Hospital (Boston), Mayo Clinic (Scottsdale), Cleveland Clinic (Cleveland), AdventHealth (Orlando), and HCA Healthcare (Houston). The study aims to evaluate the safety and effectiveness of the ELS system in robotic endoscopic submucosal dissection (ESD) procedures for the removal of colorectal lesions.

Technology and Potential Benefits

The ELS system represents a significant advancement in minimally invasive surgery (MIS). Unlike traditional methods that require larger incisions, EndoQuest's system utilizes the body’s natural orifices or transumbilical incisions to access lesions, minimizing trauma to healthy tissues. This approach could potentially allow a significant number of patients to avoid invasive operations like colectomies.
According to Dr. Todd Wilson, chief medical officer and chairman of the scientific advisory board of EndoQuest Robotics, "This technology represents the evolution we have been waiting for to finally perform endoluminal surgery, which could redefine what’s possible in minimally invasive colorectal procedures."

Pre-clinical Evidence

Pre-clinical data presented at Digestive Disease Week (DDW2024) demonstrated that the ELS System had superior procedural outcomes, a shorter learning curve, and reduced procedure time compared to conventional techniques for endoscopic dissection of lesions in the colon. These findings suggest that the ELS system could offer significant benefits in terms of outcomes, complications, and healthcare costs.

Unmet Need and Future Applications

There is a significant unmet need for improved treatment of colorectal disease in the U.S. The robotic ESD procedure offers the opportunity to demonstrate the potential benefits of flexible robotic systems in a range of procedures. While the initial focus is on colorectal lesions, EndoQuest envisions expanding the system's application to other minimally invasive surgeries, including tonsillectomies and cholecystectomies.

Market Growth and Investment

The global robotics industry is experiencing rapid growth, with surgical robotics being a key area. EndoQuest Robotics secured $42 million in financing in December 2023 to advance its endoluminal robotics technology, highlighting the investment community's confidence in the company's potential.
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Clinical Trials

Related research and studies

Highlighted Clinical Trials

NCT06133387RecruitingNot Applicable
EndoQuest Robotics, Inc.
Posted 5/13/2025

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