Exhibition - 2026
(including all MDI partners)
MDI Expo 2026 includes a large expo area, and (new!) a startup zone, where products and services will be introduced. Make sure to visit, network, and learn about all the news in the medical devices and digital healthcare community
Established in Tefen Industrial Park in Northern Galilee in 1994, 3BY is a leading provider of turnkey projects for medical device companies. We specialize in producing high-quality medical components, devices, and systems using advanced injection molding technologies and manufacturing techniques. Our OEM company provides subcontracting services, including plastic injection molding, assembly, and packaging in a certified clean-room environment.
Since 1996, A. Stein Regulatory Affairs Consulting, led by Ms. Ahava Stein, has offered the full spectrum of Regulatory, Clinical (CRO) and QMS consulting for medical devices, from FDA clearance and approvals to CE certification under MDR, as well as other international regulatory approvals (e.g., Health Canada, Japanese PMDA, Chinese NMPA, etc.).
Our interdisciplinary team of Regulatory, Clinical and QMS experts combines creativity with proactive thinking to serve a diverse client base, earning a reputation for uncompromising quality, meticulous detail, and thoroughness. From early feasibility through post-market compliance, our team guides you through the required Regulatory Submissions, Clinical Study Management, and Quality Management System compliance. We approach each project with a deep technical understanding of the client’s product and dedication to their vision, proactively advocating for the optimal Regulatory Submission and Clinical Trial Strategy, and delivering full approvals and certifications in the shortest feasible timelines, while upholding rigorous compliance.
Recognized as Israel’s leading Regulatory Affairs firm specializing in FDA and CE submissions and documentation, we bring broad device experience and a proven track record guiding and supporting clients through the regulatory maze.
Prior to the establishment of the State of Israel (1948), Englander began manufacturing tools and dies to support the needs of the fledgling industry of the young state. Since its inception, Englander has been involved in all fields of production and has specialized in manufacturing precision-stamped metal parts and tools.
Over the years, Englander has gained experience and know-how by supplying a wide range of products for the growing industry in Israel. Englander is currently exporting over 80% of its production worldwide.
Almond is professional quality management software designed for life sciences companies, developed by Gsap LTD. The software is user-friendly and incorporates insights and experience gained from accompanying hundreds of companies in the industry. It is fully validated, ensuring regulatory compliance, and supports process changes without requiring re-validation.
Alvas Rubber Products Alvas is a leading manufacturer of advanced elastomer solutions with over 70 years of experience, specializing in high-precision injection , compression molding and CNC cutting for the Defense, Medical, and High-Tech sectors. We provide comprehensive end-to-end services, ranging from R&D and custom compound development to mass production in clean-room environments. Our capabilities include utilizing Industry 4.0 technologies to deliver complex silicone and rubber components that meet strict international standards.
Aman Group is a leading IT company, providing a broad range of services and solutions in Digital, Cyber security, Data, Software Dev, Knowledge Management Blockchain and more -technology and operations, combining unmatched experience and specialized skills. In the current revolutionary times Aman uses technology and innovation to help businesses improve their performance and create value for their customers and the society. With around 2500 people we serve clients around the world with being a warm home to our employees.
We are an expert APPLICATION SECURITY TESTING & CONSULTING company.
AppSec Labs was Founded by Erez Metula in 2010 with the vision and dream of being a Global Center of excellence in the field of Application Security – the dream came true. Since our founding we have been providing penetration tested thousands of systems for hundreds of customers world-wide We have also delivered 15 trainings at the prestigious BlackHat USA conference.
WHAT WE PROVIDE:
We provide our customers with top-quality application security testing and consulting services for: Web applications, Mobile Applications, Cloud Applications, IoT & Embedded, Blockchain products and applications.
​
MEET REGULATORY REQUIREMENTS
AppSec Labs has helped hundreds of companies improve their product security and receive the desired certification needed to meet regulatory requirements such as FDA, HIPAA, PCI, SOC2, ISO 27001 and many more.
The desired product of our security process is a certification that confirms compliance to industry security standards.
Struggling with complex, ever-changing regulatory requirements? Fast-track your medical device registrations with Arazy Group’s AI-powered regulatory affairs platform. Our cutting-edge technology lets you initiate device-specific registrations in over 140 countries in seconds—not weeks. Gain instant access to customized submission files, automated compliance workflows, and real-time process management to bring your innovations to market faster, with less risk.
Ascotech Electronics Ltd has represented top global manufacturers since 1978, Providing expert support and innovative solutions such as : • ASIC Design • GaN Foundry • Silicon Caps • Optical System-In-Package • MMIC GaAs & GaN/SiC • RF Connectors • Microwave Products • Antennas
Beckhoff implements open automation systems using proven PC-based control technology. The main areas that the product range covers are industrial PCs, I/O and fieldbus components, drive technology, automation software, control cabinet-free automation, and hardware for machine vision. Product ranges that can be used as separate components or integrated into a complete and mutually compatible control system are available for all sectors. Our New Automation Technology stands for universal and industry-independent control and automation solutions that are used worldwide in a large variety of different applications, ranging from CNC-controlled machine tools to intelligent building control.
Cognit is a Human Factors Engineering (HFE) company specializing in user experience (UX) design, user research, and usability evaluations for complex systems across diverse industries. With extensive expertise in usability regulatory requirements for medical devices, our approach integrates regulatory compliance with human-centered design principles, optimizing development workflows while ensuring safe and engaging user experiences.
Cognit offers a wide range of services for medical systems, including usability strategy planning, defining user needs through user research, user interface design, use related risk analysis and regulatory-compliant usability testing – culminating in writing and submission of reports for FDA and MDR approvals.
Based in Israel and collaborating with regulatory consultants and usability labs worldwide, Cognit supports both Israeli and international companies in creating intuitive, user-friendly systems that meet regulatory requirements.
Core Human Factors (Core) is a consulting group with offices in Israel and the US. We specialize in HF testing for medical devices and healthcare systems and conduct research worldwide. Core has helped hundreds of products successfully navigate FDA review and gain CE marks, and our researchers have published dozens of publications in peer-reviewed journals. In addition to user testing, we also assist in the design of products, instructional materials, and training programs; risk analyses; user needs documentation; and ideation sessions to facilitate invention and use-centered design in healthcare and medicine.
Core's mission is to apply a human touch to all aspects of user research: serving our clients, connecting with our study participants, collaborating with our co-workers, and improving the usability and safety of products and services.
Dekra medical in Israel is 20 years active in the medical device market as a Notified Body.
Dekra is designated for all codes in MDR and IVDR.
The team of local auditors is also qualified for MDSAP and of course ISO13485.
The portfolio contains all fields and spectrum of devices in the medical field and we can handle any new device.
With branches around the world Dekra is a one stop shop in the medical field and laboratories as well.
We are a unique consulting firm that focuses on developing products that best match the physical and digital needs of the people who use them. We know that the relationship between people and the technologies they use is truly unique. By leveraging human factors & human-centered design, we are able to drastically improve the effectiveness and ease of use of innovative products and services, with the goal of seamless usability.
Global R&D Ltd is a dynamic and innovative research and development company that was established in 1995. We offer one-stop solutions for integrated multidisciplinary projects in the fields of Hardware(Analog and digital), Embedded Systems, Software and Mechanical engineering. Our team utilizes the latest technologies to provide innovative and productive solutions for our customers.
We are experienced in handling a complete project, from concept through the design and prototype to the final product delivery and serial production being an outsourcing R&D team that provides cost and time effective solutions for development projects.
We provide a risk-free complete answer for the electronics development and production of electronics for startups, and the most efficient way for any company to develop any card or system in the shortest time to market schedule.
Global R&D has ISO 9001:2015 certification and is an authorized supplier of IAI and MOD
Gsap- Accelerating healthcare companies towards approval of safe and effective products by leading quality, regulatory, engineering, validation, and clinical services.
With deep expertise in advanced technologies, including wearable devices, AI-driven products, in-vitro diagnostics, and digital health platforms, Gsap empowers innovators to navigate global regulatory landscapes and accelerate market entry.
Our tailored strategies integrate early-stage regulatory planning, in-depth risk assessments, and compliance solutions to align with each company's unique goals. By embedding regulatory and clinical insights from the outset, Gsap helps minimize delays, optimize resources, and ensure the success of groundbreaking solutions that improve patient care.
With a commitment to excellence and a proven track record, Gsap is the trusted partner for advancing cutting-edge technologies in the healthcare ecosystem.
For over 30 years, we have been assessing the conformity of medical devices and quality systems enabling medical device manufacturers to place their products on the market worldwide.
Our expertise in offering training courses tailored to your needs, the development of high-value technical and regulatory content and the support provided throughout your certification cycle are all available assets for your projects success.
HaMaDa is a prominent RA/QA/CL consulting firm possessing 15 years of Regulatory, Compliance and Clinical Affairs experience for Medical Device companies. Its professional, multidisciplinary team of 30 industry and scientific experts have been supporting leading companies in a wide range of expertise domains such as Active and Non-Active devices and Implants, In Vitro Diagnostics, Digital Health (Medical Apps, Wearable, AI and Big Data), etc.
HaMaDa has the vital experience necessary to manage the regulatory approval process, Clinical documents and processes and provides a wide range of services, for start-ups as well as established companies.
For early-stage companies, HaMaDa is crucial in defining the best strategic and tactical plans to pave the way into the market and implement these plans to achieve marketing approvals in various geographies.
For well-established companies, HaMaDa complements in-house expertise to assist with specific quality and regulatory activities, such as compliance with MDR, IVDR, MDSAP compliance preparation of documentations such as CER, PMS, PSUR, useability plans and studies, provide training for personnel or execute internal audits of the QMS, Clinical Studies and/or ISO 13485 quality system. HaMaDa may also serve as your CRO for Clinical Studies in the most advanced technological fields.
​
Horizon Electronics
Horizon Electronics Ltd. stands as a beacon of excellence in the world of power supply solutions. With a rich history spanning over 5 decades, our commitment to innovation, precision, and quality has established us as a trusted partner in diverse sectors, ranging from industrial and medical to defense and more.
Together with our Subsidiary, TITAN Power Systems, we specialize in designing, developing, manufacturing, and marketing power supply solutions that cater to the unique demands of diverse industries and applications, and are designed to operate even in the harshest environments.
Side by side with our signature products, we propose an enhanced solutions portfolio. Standing as a leading distributor, our pride extends beyond our own products. We represent the finest global brands, ensuring our clients can access the most advanced products available for each application.
Since 1958, Hever Translations has specialized in medical and healthcare translation, supporting medical device manufacturers in global market entry and regulatory compliance. We deliver end-to-end translation solutions for medical devices, including IFUs, software and UI localization, and multilingual labeling.
Our dedicated medical device teams combine medical, technical, and regulatory expertise to produce accurate, consistent, and compliant translations. All projects follow strict quality and validation processes in line with international standards, including ISO 17100, with experience across EU MDR, FDA, and global markets.
We support the full documentation lifecycle; from terminology management and multilingual UI adaptation to screenshot localization and graphic integration, ensuring content is ready for submission and use in every target market.
With a network of over 2,500 specialized translators worldwide, Hever Translations helps medical device companies reduce risk, accelerate approvals, and confidently launch products across global markets.
With more than 19 years of experience in IoT,
We have been developing IoT products since the days it was called M2M.
Our versatile services and multi-disciplinary experience can help you build your product right, right from the first step
Israel's leading provider of software development, regulation and cybersecurity services for the healthcare industry​.
A one-stop shop for medical software companies, startups, and healthcare organizations, Matrix Medika has the experience and expertise that come from helping bring over 100 successful projects to market. We help companies design and develop innovative solutions, services, and desktop, mobile, and cloud-based apps; ensure rock-solid cybersecurity and privacy in compliance with HIPAA/GDPR standards; and manage FDA/CE submissions.
Our specialization in the medical arena means you can trust us to handle V&V per IEC62304 and ISO13485 standards, risk management per ISO14971 and TIR57, preparing the software chapters for FDA 510K submission and CE certification, and registration under MDD and MDR.
We’ve helped countless products through every stage of the development and FDA/CE approval process, and we’re fully committed to ensuring client satisfaction, quick time to market and cost-effective solutions. At Medika, we’re there for you at every step of the way.
​
IceCure Medical (Nasdaq: ICCM) develops advanced liquid nitrogen-based cryoablation systems for the minimally invasive destruction of tumors by freezing them. Its ProSense System is the first and only FDA-cleared medical device for the local treatment of low-risk breast cancers for women 70 & up when combined with endocrine therapy, giving patients a safe and effective outpatient option to surgery. ProSense is currently sold worldwide with a focus on the United States, Europe, Brazil, and Asia.
Novodes delivers end-to-end embedded software quality services for organizations developing safety-critical, mission-critical, and performance sensitive systems. Our team combines deep technical expertise in embedded systems with practical experience in regulatory compliance and quality assurance.
What we do:
-
Testing: Design, implement, and automate unit and integration tests to achieve required structural coverage (Statement, Branch, MC/DC).
-
Architectural Analysis: Analyze code structure and dependencies to identif
architectural issues, technical debt, and maintainability risks. -
CI/CD Automation: Build and maintain automated pipelines integrating compilation, testing, coverage, and static analysis into continuous workflows.
-
Embedded Software Development: Develop and refactor embedded C/C++ codewith a strong focus on quality, testability, and maintainability
Pulsenmore ES is the world’s first at-home diagnostic ultrasound and telehealth platform for pregnancy monitoring, bringing imaging into the home and connecting patients with care teams remotely. Positioned at the intersection of telehealth and femtech, Pulsenmore integrates ultrasound imaging with virtual prenatal care to support earlier insights, improved continuity of care, and greater access. Clinically validated and supported by large-scale commercial adoption, the platform has enabled more than 220,000 home self-scans worldwide.
Pulsenmore is the only FDA-Authorized Home Ultrasound, approved for commercial use in the U.S., Europe, the UK, Switzerland, Australia, Brazil, Colombia, and Israel.
At Preferred Depot, we created the Operation of Things (OoT) to go far beyond simple operational support — we completely integrate into your organization, supporting everything your business needs to thrive from the ground up. From day-to-day tasks to long-term business goals — we handle your operations so you can focus your time, energy, and ingenuity into driving sales, expansion and innovation.
Ogen HR (www.ogen-hr.co.il) is a recruitment and workforce solutions partner focused on medical device companies and the high-tech sector.
We support organizations with professional recruitment, placement, and employer-of-record (EOR) services, helping teams grow efficiently in Israel.
rh Group is a global, vertically integrated manufacturing partner with over 40 years of experience in bringing complex medical devices to mass production. As one of Israel’s leading EMS providers, rh specializes in regulated medical devices manufacturing—from industrialization and NPI through advanced testing, certification, and high-volume production. With ISO 13485–certified facilities in Israel, the USA, and Europe, we enable medical device companies to scale reliably, efficiently, and compliantly from development to full-market deployment.
The Ready Group has been Israel's leading R&D service firm since 2007. The group’s wide range of technical expertise enables the next generation of technology and products of leading multinational and Israeli companies as well as innovative startups in various stages. With over 200 professionals in various technical domains, we provide software, hardware and chip development services. Our chip development services range from architecture, design and verification to full manufacturing including FPGA/ASIC design, verification, backend/layout. Our software experts are skilled in real-time and embedded systems, object-oriented programming as well as mobile and web applications and AI. We have also been working on many validation, QA and automation projects.
Solution to products ltd. (S2P ltd.) specializes in the development and production of high performance plastics, aluminum, metal and silicone parts for:
-
Electronics, telecommunication and electro optics
-
Medical equipment and accessories
-
General Consumer products
-
Electrical appliances
RS NESS Provides An Umbrella Of Services To The Life Science Industry In Different Lifecycle Stages Incorporating End-To-End Project Activities While Adhering To The Regulatory Requirements. Knowledge, Professionalism, And Dedication Lead Our Highly Qualified Team To Your Success.
RS NESS Operates In The Pharmaceutical, Biotechnological, Medical Device, Cannabis & Foodtech Industries.
Our Services Include End-To-End Solution
Singer Instruments & Control specializes in design, development and manufacturing of medical device for over 40 years.
We provide our clients full turn-key solutions: From proof-of-concept prototype design to final products serial production.
Yail Noa group is a representative of leading suppliers offering vast variety of products to the Pharmaceutical, Medical devices and Electronics industries.
Yail Pharma is a business unit of Yail Noa Group, specializes in protective packaging solutions for the Medical Device and Pharmaceutical markets.
The company supports its customers with personal high level service and strives to meet the highest standards in order to provide the most suitable solutions.
Among our customers are companies from the following markets: Cardiovascular / Neurovascular /Orthopedics/ Dental/Endo/Aesthetic/Surgical / ophthalmic/ Oncology etc.
Yail Pharma works closely with both start-up & mature companies and leads them throughout the process of developing and manufacturing the proper packaging solution.
Main Product lines :Rigid Thermoformed Blisters, Sealing Machines, Sterile Pouches/ Lids /Rolls.
Vendors represented In Israel: Nelipak, Oliver Healthcare packaging, Clariant, HAWO, Carolex, AllFlex
Systematics – Advanced 3D Printing Solutions for the Medical Industry
Systematics is a leading provider of advanced 3D printing solutions in Israel, offering cutting-edge technologies tailored for the medical sector. As an official distributor of global 3D printing brands such as Formlabs, Markforged, and HP, Systematics supplies high-precision additive manufacturing solutions for medical applications, including anatomical models, surgical guides, prosthetics, and custom medical devices.
Our expertise extends beyond hardware – we provide end-to-end support, including consulting, software integration, and training, ensuring seamless adoption of 3D printing technologies in healthcare settings. With a commitment to innovation and quality, Systematics empowers medical professionals, hospitals, and research institutions with the tools to enhance patient care and streamline medical manufacturing processes.
Visit our booth at MDI Expo to discover how our 3D printing solutions can transform medical applications.
We are a unique firm of choice for inventors, industry, and legal firms across the globe seeking an exceptional firm for their IP needs.