We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress
Sign In
Advertise with Us
Sekisui Diagnostics UK Ltd.

Download Mobile App




First-Of-Kind Endoscopic Ultrasound Technology Offers Groundbreaking Approach to Patient Safety

By HospiMedica International staff writers
Posted on 03 Jan 2024
Print article
Image: This first-of-its-kind endoscopic ultrasound technology has received US FDA 510(k) clearance (Photo courtesy of EndoSound)
Image: This first-of-its-kind endoscopic ultrasound technology has received US FDA 510(k) clearance (Photo courtesy of EndoSound)

Endoscopic Ultrasound (EUS) is a minimally invasive technique used to diagnose conditions of the gastrointestinal (GI) tract and nearby organs. EUS combines the capabilities of endoscopy and ultrasound to generate detailed visuals of the digestive system, including organs like the pancreas, liver, and gallbladder. Typically, over 95% of EUS procedures are performed in hospital environments, but many patients could benefit from undergoing these procedures in more convenient settings like ambulatory surgery centers (ASC). Now, a first-of-its-kind EUS technology with a groundbreaking approach to patient safety has the potential to shift the site of care to more efficient and preferable settings like ASCs.

The EndoSound Vision System (EVS) from EndoSound Inc. (Portland, OR, USA) is an innovative EUS device designed to attach to upper gastrointestinal endoscopes and seamlessly integrate into the existing ecosystem of any endoscopy center. The EVS marks a substantial advancement in medical technology, particularly targeting the risk of infections linked to the complex cleaning of endoscope elevators. The system is set to redefine EUS with its affordability, enhanced safety, and capability to convert a standard upper GI endoscope into an EUS system, thereby broadening access to this vital diagnostic and therapeutic procedure.

The FDA has granted 510(k) clearance to the EVS, after recognizing it as a Breakthrough Device in July 2021, highlighting its innovative approach to patient safety, cost-effectiveness, and expanding access to essential healthcare services. This FDA endorsement confirms the system's safety and efficacy, reinforcing EndoSound's dedication to advancing healthcare through innovative solutions.

"We are thrilled to receive 510(k) clearance for our EVS, a testament to the dedication and innovation of the entire EndoSound team," said Dr. Stephen Steinberg, President and CEO at EndoSound. “This milestone underscores our commitment to advancing medical technology and improving patient outcomes. With the EVS, we aim to not only enhance the safety of endoscopic procedures but also contribute to expanding access to care for patients worldwide.”

Related Links:
EndoSound Inc. 

Gold Member
STI Test
Vivalytic Sexually Transmitted Infection (STI) Array
Gold Member
SARS‑CoV‑2/Flu A/Flu B/RSV Sample-To-Answer Test
SARS‑CoV‑2/Flu A/Flu B/RSV Cartridge (CE-IVD)
Silver Member
Wireless Mobile ECG Recorder
NR-1207-3/NR-1207-E
New
Autoclavable Camera System
Precision AC

Print article

Channels

Patient Care

view channel
Image: The newly-launched solution can transform operating room scheduling and boost utilization rates (Photo courtesy of Fujitsu)

Surgical Capacity Optimization Solution Helps Hospitals Boost OR Utilization

An innovative solution has the capability to transform surgical capacity utilization by targeting the root cause of surgical block time inefficiencies. Fujitsu Limited’s (Tokyo, Japan) Surgical Capacity... Read more

Health IT

view channel
Image: First ever institution-specific model provides significant performance advantage over current population-derived models (Photo courtesy of Mount Sinai)

Machine Learning Model Improves Mortality Risk Prediction for Cardiac Surgery Patients

Machine learning algorithms have been deployed to create predictive models in various medical fields, with some demonstrating improved outcomes compared to their standard-of-care counterparts.... Read more

Point of Care

view channel
Image: The Quantra Hemostasis System has received US FDA special 510(k) clearance for use with its Quantra QStat Cartridge (Photo courtesy of HemoSonics)

Critical Bleeding Management System to Help Hospitals Further Standardize Viscoelastic Testing

Surgical procedures are often accompanied by significant blood loss and the subsequent high likelihood of the need for allogeneic blood transfusions. These transfusions, while critical, are linked to various... Read more
Copyright © 2000-2024 Globetech Media. All rights reserved.