Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. With a portfolio of leading, science-based offerings in diagnostics, medical devices, nutritionals and branded generic pharmaceuticals, Abbott serves people in more than 150 countries and employs approximately 99,000 people.
For over 40 years, Anomet Products has focused exclusively on manufacturing innovative clad-metal wire composite solutions that deliver optimized performance for the most demanding applications. Our goal has always been to provide superior material quality, product value and customer satisfaction through service and support that far exceed expectations. We’re proud that this unwavering commitment has fostered strong, collaborative partnerships with leading OEMs across an extremely diverse range of business sectors, including aerospace & defense, automotive, battery & fuel cell technology, energy production (oil & gas), appliances, corrosion protection, industrial, electronic, superconductors, medical devices and electrochemical.
ArKco Sales, Inc is a manufacturer sales representative for the upper Midwest five state territories. The territory consists of Minnesota, Western Wisconsin, Iowa, Nebraska, North Dakota, and South Dakota.
ArKco core markets include: Transportation, HVACR, Industrial, Medical, Power Generation, IT/Server, and Military.
The mission of ArKco Sales Inc. is to provide professional field sales service for our principals, customers, and distributor partners. We provide local relationship management for global electro-mechanical component and assembly solutions.
Atlas Vac, in addition to standard units, offers an All Electric Model medical device tray sealer. The All Electric Model 1830S provides supreme down-force control unmatched by any other pneumatic sealer. Precision sealing forces are repeatable to the tightest tolerance of any tray sealer available. All Atlas Vac sealers are available with: OSHA or ISO13849-1 Cat 3 compliant light curtain safety systems; Bar code recipe and UDI input for lot tracking, Audit Trail data output, Direct data printing on sealed trays or traditional labels, Direct Down-Force Measurement, Auto Electric Shuttle technology for ultrasmooth movement; calibration ports for all parameter readings; heaviest cross section heater design for even heat distribution; and anodized single-piece CNC precision tooling nests with molded gaskets. All Atlas Vac sealers are PLC controlled for correct validation of processes.
BlackHägen Design is an interdisciplinary, R&D consultancy. At our core, user-centered methodologies drive innovation and sustainable product development of safety-critical devices and systems. This foundation of rigorous processes enables BH to be usability design experts. Our strategic relationships strive to discover, design and develop products and procedures which enhance technical, clinical and lifestyle conditions. We have cultivated long-term partnerships with start-up entities and market-leaders alike, enabling profitability and market-share growth through a highly collaborative approach. Our systematic methodology for translating research insights into requirements and synthesizing innovation has contributed to over 100 patents and trade secrets for our clients.
CSA Group is an internationally accredited provider of testing & certification services and a global leader in healthcare systems conformity assessment services, helping manufacturers’ access markets around the world. We test and certify medical products to required standards – including IEC 60601 and IEC 61010 – as well as offer cybersecurity assurance programs. For 100 years, CSA Group has helped clients demonstrate compliance with relevant standards for their products, helping them to reach patients and healthcare professionals around the world.
Medical device manufacturers look to Element’s ISO 17025-accredited testing services for evaluating their materials and products in the orthopedic, cardiovascular, pharmaceutical and diagnostic/therapeutic equipment industries. As your trusted testing partner, we make certain that your products are safe, quality, compliant and fit for purpose.
The engineering professionals at Element are experienced in every stage of testing – from test protocol development to material evaluation and failure analysis. A wide variety of testing services for medical devices is available, including mechanical testing, product qualification, material characterization, packaging testing, EMC/EMI testing, pharmaceutical and microbiological analysis.
With extensive knowledge of the commercialization process, regulatory requirements and scientific trends in the Industry, Eurofins Medical Device Testing offers regulatory compliance expertise and experienced GMP/GLP/ISO 17025 testing to ensure rapid turnaround times with the highest level of service and most advanced technologies for your analytical chemical, microbiological, biocompatibility, electrical, mechanical and package testing needs.
Our scientists and engineers have been assisting companies, large and small, with developmental testing for more than 25 years; and our global network of 16 laboratories in North America, Europe and Asia Pacific provide extensive capacity and the highest level of instrument technology with a full scope of testing services.
Since 1999, Fang Consulting, Ltd. has provided specialized Regulatory Affairs consulting, Quality System consulting, Clinical consulting, as well as device fulfillment, primarily for the medical device industry. Our team is comprised of principal, senior and junior consultants who have a working knowledge of and expertise in the most current global regulations and certifications and work closely with global government agencies. Visit www.fangconsulting.com to learn more about our services.
Green Hills Software is the largest independent embedded software provider. With the most safety and security certifications and the best track record for solving embedded problems, Green Hills Software has been leading the embedded world since 1982.
Jordi Labs was founded in 1980 to provide the highest quality analytical services, polymer-based HPLC columns and packing media in the industry. Today, we are worldwide leaders in extractable & leachables testing, particulates & residue analysis, polymer analysis and more. Jordi Labs provides contract analytical services with a special emphasis on chemical identification and liquid chromatography products. As a family company, we take pride in the production of all of our products and analytical service offerings. Customers in nearly all industries are currently using our columns and packing media products worldwide. It is our goal to help our customers overcome their analytical challenges by providing excellent products and personal assistance from our highly trained staff.
MedAcuity is the go-to, U.S. based software engineering firm for global MedTech companies. We are an ISO 13485:2016 certified organization with over a decade of experience delivering software development solutions for all classes of medical devices. MedAcuity has an elite group of software engineers who specialize in MedTech development. Our approach is focused on solving complex software problems and providing next-generation solutions to assist MedTech companies in delivering innovative products to market.
Medidata is leading the digital transformation of life sciences with the world’s most-used platform for clinical development, commercial and real-world data. Powered by artificial intelligence and delivered by #1 ranked industry experts, the Intelligent Platform for Life Sciences helps pharmaceutical, biotech, medical device companies and academic researchers accelerate value, minimize risk and optimize outcomes. Medidata serves more than 1,000 customers and partners worldwide and empowers more than 100,000 certified users every day to create hope for millions of patients. Discover the future of life sciences.
Created in 1979 by the healthcare technology industry, Medmarc’s purpose is to be the superior provider of liability insurance and related risk management solutions and to support the development, testing and delivery of medical products that save lives and improve the quality of life. Through collaboration with our parent company, ProAssurance, and our clinical trial industry experts, we provide a single source of innovative healthcare liability insurance solutions to the life sciences companies we serve. From ideas and prototypes to the reality of commercialization and success – We can Meet Your Changing Needs. Call me, George Ayd (800) 356-6886, to discuss the cost of insurance coverage, what coverages are needed and when, for your business plan.
Perforce is a leading provider of enterprise-scale software solutions to technology developers and development operations (“DevOps”) teams requiring productivity, visibility, and scale during all phases of the development lifecycle. Enterprises across the globe rely on its Agile planning and ALM tools, developer collaboration, static code analysis, version control, and repository management solutions as the foundation for successful DevOps at scale. Perforce is trusted by the world’s most innovative brands, including NVIDIA, Pixar, Scania, Ubisoft, and VMware. Perforce has offices in Minneapolis, MN, Alameda, CA, Mason, OH, Boston, MA, the United Kingdom, Finland, Sweden, Germany, India, and Australia, and sales partners around the globe.
At Propel, we’re building modern cloud Product Lifecycle Management, Product Information Management and Quality Management software to help propel your digital transformation. Whether you’re at an established company dealing with potentially more nimble competitors, or you’re ramping a young startup and scaling your business, Propel’s cloud software can help.
R&Q exists to improve people’s lives; the patients, our clients and our team members. R&Q helps bring more safe and effective medical devices to market for both medical device companies and combination product companies. Leveraging our deep industry experience, our company provides solutions that help improve the world. Drawing on expertise across the entire medical device product lifecycle, R&Q is uniquely positioned to present a range of strategic and tactical options and execute on the solution that best suits our clients’ individual regulatory and quality needs. R&Q’s headquarters are in Pittsburgh, PA with additional offices in Cleveland, OH, Boston, MA, Minneapolis, MN and Philadelphia, PA. From these offices, we service both nationally and internationally. R&Q is 100% women owned and is a certified Women’s Business Enterprise by WBENC.
S3 Connected Health design and develop award-winning connected medical devices, systems and solutions for our medtech partners. We specialize in implantable, wearable, and hospital-based medical devices; SaMD (Software as a Medical Device) and IoMT (Internet of Medical Things) based solutions.
Our scalable, secure, regulatory-compliant systems enable devices to capture real-world data and create insights to enhance operational efficiency, improve patient services, increase clinical effectiveness and demonstrate value.
No matter where your company is on its journey, we can help. From full market analysis and concept ideation, to design and development of industry-leading solutions, through to acting as legal manufacturer.
SAES Group is an advanced materials company: our know-how is focused on gas-solid interactions and gettering, release of high purity vapours, shape memory and superelastic materials and addition of specialized functionalities to polymer systems.
SAES Group provides a very large portfolio of active edge sealants, active transparent fillers, dispensable getters, specially tailored to address customers’ specific device designs and processes.
Toxikon is a preclinical contract research organization. We contract and partner with biotech, pharmaceutical and medical device industries to deliver exceptional product development services from concept to final product.
Triple Ring is an imaginative research and development firm that, together with our clients, solves critical, often complex technical challenges. We work across the development process in regulated markets including medical devices, in vitro diagnostics & life science tools, imaging, and industrial applications.
Founded in 2005, our team now includes over 100 experienced scientists, engineers, and market experts. We have worked with over 200 clients ranging from entrepreneurs to large OEM’s both inside and outside the US and completed over 500 projects spanning technology assessments and brainstorming to complete product development.
TUV Rheinland provides certification services to EN ISO 13485, EU Directives and ISO 13485:2003 under CMDCAS. TUV Rheinland is also accredited by OSHA as an NRTL and offers product safety testing for electrical and medical products. Additional services offered by TUV Rheinland include RoHS/REACH, EMC/wireless/radio, Cybersecurity and Market Access.
Vascudyne Inc., a University of Minnesota start-up company, is on a mission to become the world’s leading center of excellence and commercial manufacturer of an innovative in-vitro grown extracellular matrix. We provide this unique 100% biological ECM material to our clients while also developing state of the art devices based on this promising technology.
Vascudyne’s technology is based on discoveries by University researcher Robert Tranquillo, Ph.D., professor in the departments of Biomedical Engineering and Chemical Engineering & Materials Science in the College of Science and Engineering, and his team.
The Vascudyne’s decellularized collagenous tissue is grown in a simple bioreactor from human dermal fibroblasts in fibrin gel. The resulting tissue has biological and mechanical properties very similar to native tissue which passively recelluralizes and remodels without immunogenic reactions. This completely biological, off-the-shelf biomimetic material has the potential to move medical device technologies beyond the supply, durability, and hemocompatibility limitations of current synthetic and native tissue options.
Velentium offers world class expertise in software, usability, cybersecurity, electrical, and mechanical development for medical devices. Our decades of experience, solid program management and systems engineering will ensure the success of your product.
Ximedica is a full-service ISO 13485-certified and FDA-registered medical device and diagnostics product development firm. For 30 years Ximedica has provided a unique growth platform enabling organizations to successfully deploy medical technology products into the market. Its headquarters are in Providence, R.I., with offices in Hong Kong, Minneapolis, San Francisco and Silicon Valley. In November of 2014, SV LifeSciences, a Boston-based private equity firm, acquired a majority stake in Ximedica, enabling the company to execute its growth strategy.
Xometry is the largest online marketplace for custom manufacturing, connecting companies with manufacturing solutions through proprietary AI algorithms. Xometry provides on-demand manufacturing and industrial supply materials to a diverse customer base, ranging from startups to Fortune 100 companies. Xometry offers CNC Machining, 3D Printing, Sheet Metal, Injection Molding and more.