openPR Logo
Press release

IEI Unveils FDA-Certified EndoCap-3588 for Legacy Endoscopy Upgrades

06-27-2025 08:52 AM CET | Health & Medicine

Press release from: IEI Technology USA Corp.

IEI Unveils FDA-Certified EndoCap-3588 for Legacy Endoscopy

IEI Technology USA Corp. announced the launch of the EndoCap-3588, an all-in-one video recorder and capture system that enhances the digital recording of traditional endoscopes, extending the lifespan of existing equipment during upgrades.

Featuring a high-performance processor with quad-core Cortex-A76 and quad-core Cortex-A55 up to 2.4GHz, the EndoCap-3588 integrates an 8-inch 10-point multi-touch panel, 4K HDMI input and 4K/8K output, and user-friendly software certified by the FDA (FDA K152034). The device enables medical professionals to digitally capture and archive high-resolution videos and still images during surgical and endoscopic procedures with minimal setup.

"The EndoCap-3588 brings efficiency and precision to legacy endoscopy systems without requiring full system replacements," said Eric Hsieh, General Manager of IEI USA. "Its intuitive interface, robust DICOM 3.0 integration, and advanced video features support seamless digital transformation across platforms."

The system supports real-time 60 FPS recording, onboard 8GB LPDDR4x memory, and a pre-installed 4TB NVMe SSD, enabling medical teams to store and transfer large imaging files quickly. Dual front USB 3.0 ports provide flexible data export, while GPIO-integrated foot pedal control allows for sterile, hands-free operation.

Key Features:
• Quad-core Cortex-A76 and quad-core Cortex-A55, up to 2.4GHz
• 8-inch 10-point multi-touch PCAP touch panel
• 6 x USB (4 x USB 2.0 / 2 x USB 3.0)
• HDMI in up to 4K@60FPS
• 2 x HDMI output (1x 8K@60Hz / 1x 4K@60Hz)
• Onboard 8GBLPDDR4x Memory
• FDA-certified software with user-friendly UI

The EndoCap-3588 is available now and is ideal for surgical rooms, outpatient centers, and endoscopy suites seeking to upgrade existing equipment without compromising on image quality or workflow efficiency. For more information about the EndoCap-3588, visit https://bit.ly/43AHANz or contact our sales team at solutions@usa.ieiworld.com.

About IEI Technology USA Corp.

IEI Technology USA Corp. is a leading provider of industrial computer solutions, committed to delivering cutting-edge solutions for various industries worldwide.

IEI Technology USA Corp.
138 University Parkway, Pomona, CA 91768
solutions@usa.ieiworld.com
https://www.ieiworld.com/en/

IEI Technology USA Corp. builds up the business as a leading industrial computer provider, and turns to artificial intelligence and networking edge computing. IEI's products are applied in computer-based applications such as factory automation, computer telephony integration, networking appliances, security, systems, and in fields like AI, IoT (Internet of Things), national defense, police administration, transportation, communication base stations and medical instruments. IEI continues to promote its brand products as well as serving ODM vertical markets to offer complete and professional services.

IEI is alliance with Intel, Microsoft, Amazon to offer a complete intelligent system with various options, including kinds of hardware devices, different operating systems, multiple applications, private/hybrid/public cloud computing, and data storage and security for developing integrated solutions, collaborating new applications, and expanding the markets.

IEI strives to achieve the ultimate aim of IoT and AI, and to create comfortable and convenient living spaces for human beings by using advanced technologies.

This release was published on openPR.

Permanent link to this press release:

Copy
Please set a link in the press area of your homepage to this press release on openPR. openPR disclaims liability for any content contained in this release.

You can edit or delete your press release IEI Unveils FDA-Certified EndoCap-3588 for Legacy Endoscopy Upgrades here

News-ID: 4084011 • Views:

More Releases from IEI Technology USA Corp.

IEI Launches IMB-AM5 micro-ATX Motherboard Featuring AMD RyzenTM 7000/8000G/9000 PHX1 Series Processors for High-Performance Industrial Applications
IEI Launches IMB-AM5 micro-ATX Motherboard Featuring AMD RyzenTM 7000/8000G/9000 …
IEI Technology USA Corp. has announced the release of its new IMB-AM5, a powerful micro-ATX industrial motherboard designed to meet the increasing demands of edge computing, machine vision, and AI-based industrial applications. Powered by AMD RyzenTM 7000, 8000G PHX1, and 9000 Series desktop processors, the IMB-AM5 offers high-speed DDR5 memory, advanced graphics support, and flexible expansion in a compact footprint. Engineered for performance and reliability, the IMB-AM5 supports up to 192GB

More Releases for FDA

FDA Compliant Blood Storage and Preservation
Accsense Monitoring System Automates Data Archive and Alarming CAS DataLoggers provided the temperature alarming and monitoring system to a hospital blood bank looking to replace their old paper chart recorders as they became unreliable and spare parts were harder to find. For proper blood storage and preservation, the lab’s medical units needed to maintain storage temperatures between 2°C to 6°C (36°F to 43°F), given the perishability of blood components. The facility
Peyronie’s Disease Market - Only FDA approved product
The market is dominated by a single player, Endo International plc who sells the only FDA approved Peyronie’s disease product. In May 2015, the American Urological Association presented the first ever treatment guidelines for Peyronie’s disease recommending the use of Xiaflex. Furthermore, the company is creating awareness through its “Ask About the Curve” campaign. Also, reimbursement from the U.S. insurance providers will boost the demand for this product. The product
FDA grants orphan drug status to Vicore
US Food and Drug Administration has awarded Vicore Pharmaceuticals with orphan Drug designation for the treatment of Idiopathic Pulmonary Fibrosis (IPF). FDA’s Orphan Drug Designation program provides certain incentives for companies developing therapeutics to treat rare diseases or conditions, defined as those affecting less than 200,000 individuals in the U.S. A drug candidate and its sponsor must meet several key criteria in order to qualify for, and obtain, orphan drug
New FDA Design Control Training Courses
Salt Lake City, Utah - February 23 2017 - Procenius Consulting is a medical device consulting firm specializing solely in medical device design controls regulation (21 CFR 820.30). Announcing New Design Control Training Courses Procenius Consulting has just launched two new training courses covering basic and advanced topics of medical device design control regulation. These courses focus on compliance, practical implementation and industry best practices techniques for developing or improving a
fda online training
GRC Training Solutions provides end-to-end FDA compliance solutions for those companies who want to maximize security, minimize operational costs, improve staff productivity and stay on top of all their compliance documentation. GRC Training Solutions boasts a team of experts and specialists who have a proven track record in working with the biotechnology, medical device, diagnostic and pharmaceutical fields. Our team will work with you closely and develop solutions that meet
11-09-2016 | Science & Education
GRCTS
FDA online training
Description: Device firms, establishments or facilities that are involved in the production and distribution of medical devices intended for use in the U.S are required to register annually. Most establishments that are required to register with the FDA are also required to list the devices that are made there and the activities that are performed on those devices. Initially, FDA issued a 28-page Proposed Rule that would amend its regulations regarding