Design Molded Plastics, with more than 30 years of experience in custom plastic injection molding, is committed to using our engineering and manufacturing skills to offer innovative solutions for our clients. We are able to provide knowledgeable recommendations that lead to our customers’ success thanks to our extensive experience in a variety of applications and industries. With state-of-the-art production facilities, sophisticated tools, and experienced process engineers at our disposal, we are highly proficient in executing intricate, tailored, and demanding projects with accuracy and efficiency.

Based in Ohio, Progressive Molding Technologies, Inc. offers custom injection molding services as a service-oriented alternative for plastic injection molded products and services. We focus on precision injection molding of engineering plastics with close tolerances. With our scientific processing methods and automated cell-molding approach, we can enhance the value and cut costs for your plastic parts production. Additionally, Progressive provides comprehensive engineering services for developing parts and products. No matter if you require a single component design or a sophisticated electro-mechanical assembly, we can transform your ideas from concept to mass production. The engineering team at PMT has extensive experience in product design, prototyping, engineering analysis, and manufacturing, drawing on a diverse range of manufacturing and engineering disciplines.

Current Concept DesignWorks presents an overview of its product ecosystem (AccessEmulator, ReaderRouter, ReaderHub, Wiegand Calculator, Ordering Info, FAQ) along with recent and historical updates to the ReaderRouter product line, and an emphasis on design services. It highlights new features such as USB connectivity and LED diagnostics, outlines company capabilities in product development and testing, and notes the company’s history of access control solutions and customization for varied installation needs.

GET Engineering is a complete in-house design, engineering, and manufacturing firm (ISO 9001:2015) located in El Cajon, CA, offering custom electronics, cable assemblies, and legacy-to-new technology transitions for commercial, industrial, and MIL-SPEC applications, with a focus on rapid turnaround, software support, and platform-independent solutions to support defense and commercial customers. Key Points GET Engineering provides end-to-end design, engineering, and manufacturing services from a single facility. The company is ISO 9001:2015 registered and adheres to IPC-A-610 and WHMA-A-620 standards. It has a legacy of serving the U.S. DoD, FMS, and commercial contractors since 1982, with over 40 years of expertise. GET offers obsolescence solutions, including form-fit-function replacements and legacy-to-new network integrations. It provides conversion devices to connect legacy protocols to Ethernet-based networks. The firm supports transitioning from copper to fiber for secure, cost-effective networking. In-house engineering and production enable custom electronic product design, testing, and integration. Rapid turnaround is achieved by stocking thousands of components, cables, and chips and maintaining legacy parts. Ongoing software and firmware support is provided directly by GET’s engineers, with customer access to programmers. GET delivers custom solutions beyond COTS, including software development, custom cables, and on-site consulting. Platform-independent software for NTDS adapters allows code written for one OS to run across others, with upgrades available on the GET site.

NOVO Engineering offers two decades of transforming new technologies into innovative products through comprehensive product development services from concept to launch, supported by a world-class on-demand engineering team. Their approach emphasizes breadth across industries and technologies, a focus on innovation and problem-solving, and a proven track record of consistent performance through extensive prototyping, testing, and a convergent development process.

AJ Medical Manufacturing is a leading FDA-registered and ISO 13485-certified medical device contract manufacturer based in Houston, Texas. Our state-of-the-art facility combines advanced technology with a vertically integrated manufacturing approach, enabling us to deliver custom medical devices and components with exceptional precision and reliability. By leveraging our agile manufacturing processes, we help our partners reduce inventory costs and accelerate time-to-market, without compromising on quality. At AJ Medical, we thrive on engineering challenges, embrace diversity, and are committed to producing high-quality, Made-in-USA medical devices that meet the exacting standards of our clients. Partner with AJ Medical Manufacturing for custom medical device solutions that are efficient, compliant, and designed to support your success in the healthcare industry.

In addition to our core product portfolio, we collaborate with entrepreneurs and early-stage companies to deliver comprehensive product development support, intellectual property guidance, strategic regulatory planning, and scalable commercial manufacturing solutions. Our multidisciplinary designers and engineers turn innovative ideas into high-performance products that look exceptional and function flawlessly.

DesignPlex Biomedical, founded in 2015, was created to address a critical need in medical device development for early-stage implanted blood pumps, artificial hearts, and related peripheral equipment. Over the years, the company has broadened its expertise to support advanced technologies including optogenetics for neuromodulation, medication dosing systems, reliability test fixtures, wound care innovations, pacemaker management tools, heart simulators, and specialized solutions for fat grafting. During the COVID-19 pandemic, DesignPlex also contributed to public health efforts by developing face shields, face masks, ventilator components, and antimicrobial coating technologies. Today, DesignPlex Biomedical is proudly ISO 13485:2016 certified for the design and manufacturing of active implantable medical devices (AIMDs), reinforcing its commitment to quality, safety, and regulatory excellence in the medical device industry.

Evolve Medtech Partners is a leading medical device development company and innovation engine dedicated to transforming ideas into market-ready solutions. We collaborate closely with inventors, physicians, early-stage medical device companies, established organizations, and investors to accelerate concepts from initial discovery through licensing, acquisition, or full commercialization. Early-stage ventures are launched, supported, and co-located within the Evolve facility to streamline development and scale efficiently. Our team delivers expert leadership across every phase of medical device product development, leveraging extensive industry experience and a proven track record for rapidly advancing technologies to market. With a broad network of internal and external partners, Evolve provides deep capabilities in product development, intellectual property strategy, regulatory and quality compliance, manufacturing, commercialization, clinical strategy, and business development. Evolve operates a fully compliant ISO 13485:2016 and 21 CFR 820 quality management system, ensuring that every innovation is developed with the highest standards of safety, effectiveness, and regulatory readiness.

We specialize in creating breakthrough healthcare products and building commercially successful healthtech businesses that transform patient care and improve lives worldwide. With a team of 300+ multidisciplinary experts, we provide end-to-end support across the full product lifecycle—from product design and engineering to manufacturing, scale-up, and commercialization. Our integrated capabilities help clients accelerate the development of innovative solutions for the diagnostics, life sciences, and medical device industries. In addition to our development services, we make strategic investments in high-potential global healthtech companies, enabling them to achieve stronger market adoption, drive commercial growth, and build long-term value through collaborative partnerships.

At Amphenol CIT, solving customer challenges is our core mission. Backed by more than 80 years of industry expertise, we combine engineering agility with global manufacturing capabilities to deliver complete end-to-end connectivity solutions. Our broad product portfolio spans wire and cable assemblies, specialty connectors, precision contacts, SATCOM technologies, and fully customized engineering services. Each solution is designed to meet complex regulatory, environmental, and integration requirements—empowering our customers to innovate and succeed in today’s rapidly evolving marketplace.

Accudata Solutions provides specialized biostatistics and clinical data management support for small- to medium-sized pharmaceutical, medical device, and biotechnology companies. We deliver timely, actionable guidance on clinical study design, data management strategies, statistical analysis, and quality control methods, ensuring your development program stays efficient and compliant. Our flexible, personal approach fosters long-term client relationships built on clarity, collaboration, and communication—without unnecessary statistical jargon. Doug’s unique strategic partnership model helps you evaluate your project needs, understand critical options, and choose the most effective path forward. By focusing early on regulatory and scientific end-requirements, he guides you toward a streamlined and strategic route to approval.

ECA is the trusted partner for organizations moving to single-use, Surgery-Ready Solutions™. We provide the complete, end-to-end pathway to bring a surgical procedure kit or single-use sterile instrument from concept to full-scale production. As a true single-source provider, we streamline every step—from ideation and engineering through manufacturing, packaging, sterilization, and fulfillment—helping you rapidly launch high-quality, compliance-ready surgical solutions with confidence.

Medical Development Services, Inc. (MDS) provides world-class technical services to medical device manufacturers and pharmaceutical companies across the globe. As a fully virtual, telework-based organization, MDS leverages advanced electronic commerce systems to streamline workflows, reduce project timelines, and lower costs for clients. Since 1997, the U.S. Department of Commerce in Washington, D.C. has recognized MDS as an industry pioneer in delivering Internet-based technical services. Over the years, MDS has also contributed to the development of United States, California, and San Diego energy and workplace policies, reinforcing its role as a leader in innovation and remote technical support.

Viant positions itself as a medical device manufacturing partner with a comprehensive, clinically informed approach across multiple markets, including orthopedics, surgical technology, cardiac and interventional, drug delivery, bioprocessing, bioelectronics, diagnostics, and respiratory/patient care, offering end-to-end capabilities in plastic and silicone molding, manufacturing, assembly, filling, packaging, and sterilization management to deliver high-quality devices that improve patient and provider outcomes.

Cirtec Medical positions itself as a vertically integrated partner for OEMs and startups, offering end-to-end services from concept to commercialization to accelerate innovation, reduce costs, and shorten time-to-market, underpinned by core values of collaboration, transparency, innovation, and quality, with a global footprint of nine facilities and over 300,000 sq ft of production space.

Medicatech USA® presents itself as a leading American-made provider of digital radiography solutions for both human medical and veterinary markets, emphasizing innovative, high-quality, and competitively priced DR systems, acquisition platforms, and PACS software, with a strong commitment to customization, customer support, and rapid nationwide growth. Key Points Medicatech USA designs and manufactures digital radiography systems, acquisition platforms, and PACS software in the United States. The company serves both Human Medical and Veterinary markets and has been active since 2005. Core value propositions include American-made quality, ongoing innovation, and high-definition imaging at competitive prices. Exceptional customer support spans installation and ongoing technical assistance. The company emphasizes customization, offering engineers who modify and tailor products to client needs. Medicatech positions itself as the fastest-growing digital radiography provider in the U.S. due to its focus on innovation and customer-centric solutions. A wide product catalog covers DR panels, medical and veterinary systems, and various X-ray and detector technologies, including several wireless and tethered options.

Medeologix positions itself as a one-stop shop delivering fast, cost-effective, and high-quality medical device development and manufacturing through integrated technologies, lean smart-manufacturing, and agile project management, all supported by a global quality framework and a mission to be the most dependable partner in bringing life-saving innovations to market worldwide.

The document presents a succinct overview of R&D Medical Products, highlighting a globally experienced team and a mission to pioneer medical electrodes and hydrogels for OEM partnerships, while emphasizing a customer-centric project process, long-standing client relationships, and a firm commitment to quality and regulatory readiness. Key Points The company leverages a worldwide experienced team, including named professionals. Mission focuses on pioneering medical electrodes and hydrogels for innovative OEM partnerships. The organization positions itself as a contract manufacturer for the “patients of tomorrow.” Vision centers on creating, developing, and manufacturing electrodes for niche markets. Core values include trust, loyalty, integration, reliability, integrity, teamwork, and stability. The project approach emphasizes proactive design review for manufacturability, regulatory, and IP considerations beyond a simple quote. The process workflow includes discuss, review, and build stages to ensure alignment with technical and commercial requirements. Since 1997, the company has sustained long-term relationships with clients, maintaining operations at the same location and ownership. Quality is integral, with a culture of problem-solving and regular audits by independent bodies and customers.

Design Catapult Manufacturing Inc. (DCM), a spin-off from Design Catapult Inc. (DC), specializes in production manufacturing for medical devices since 2017, holding ISO 9001 and ISO 13485 certifications along with FDA registrations, and is committed to quality, on-time delivery, regulatory compliance, and continuous improvement under a robust Quality Management System. Key Points DCM focuses on production manufacturing for medical devices, operating since 2017. DC has been established since 2002 and serves as the design partner, capable of taking concepts to production. DCM holds ISO 9001 and ISO 13485 certifications specific to medical device manufacturing. FDA registrations are maintained by DCM, ensuring regulatory compliance in the United States. The company emphasizes meeting customer expectations through impeccable quality and timely deliveries. A commitment to sustaining a compliant Quality Management System is highlighted. The leadership team includes a President/Founder, HR Manager, Operations Manager, and Quality Manager.