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15+ years of IT excellence Over 1,200 clients worldwide We keep creating digital solutions that have a real measurable positive impact. Companies we work with grow 5-10x due to strategic planning, smart execution, and high-performance technology that speeds up results. With our streamlined workflows, projects can be finished in as fast as 70%, allowing brands to scale with assurance and surety. With a 98% client satisfaction rate, we remain core focused on reliability and innovation and have made it our mission to design digital experiences that purposefully disrupt the market, enabling businesses to break through any expected barriers.
They chose clarity, They chose progress, They chose AQLIX




















Delivering reliable, compliant and future-ready healthcare innovations.
We take early clinical ideas through to first-on-patient designs by applying UX research, regulatory foresight and technical feasibility frameworks. U.S. based clients get validated, secure and deployment ready ideas, along with actionable documentation as well as preliminary prototyping recommendations.
Our engineers manufacture precise prototypes that are powered by CAD and the unmatched accuracy of materials testing and rapid 3D fabrication. U.S. healthcare businesses receive minimized iteration costs, faster cycles and regulatory harmonized prototypes architected for reliable performance and scalability.
Aqlix is FDA, ISO & US health care regulations compliant on all devices. Such product safety assessments reduce the risk of redesign, speed approval cycles and give American companies opportunities to go confidently to market with compliant products.
We design, ergonomic, modern look and safety-based devices for clinical areas. These convenient designs enhance patient comfort and streamline use for health professionals in the hospital, clinic or laboratory.
We build smart monitoring, automation and clinical data connection capabilities into medical devices. US customers benefit from strong and reliable software features that enrich real-time visibility as well as end-user performance.
Elaborate and accurate CAD profiles and 3D data limit the number of design errors - cutting short cycles - while at the same time assisting with right-first-time manufacturing. This provides customers with a cost-effective engineering workflow, and fast prototype-to-production changeovers.
We conduct rigorous human-factor tests to verify safety, efficacy and ease of use. The result for clients is better clinical outcome, compliant admission and greater uptake.
Aqlix manages clients from material selection to vendor search, mold and production planning. U.S. companies gain access to consistent, scalable and quality-centric manufacturing.
We make continuous updates and product enhancements to adapt to performance, security and the long term clinical value.
Every medical product is uniquely developed to meet U.S. clinical needs.
Our designs leverage advanced technologies ensuring scalability and long-term relevance.
All products follow FDA, ISO and U.S. healthcare compliance standards.
Projects are executed quickly without compromising precision or quality.
Our U.S.-focused engineering teams deliver measurable, dependable results.
Clients achieve faster market entry, improved usability and up to 10x operational efficiency gains.
Interested?
Contact us to discuss and collaborate on your project!


For healthcare companies looking for innovative, patient-safe and market-ready solutions, they would want to find reputable Medical Product Development Companies in the U.S. Aqlix IT Solutions offers comprehensive development support: clinical insight, engineering precision and regulatory know-how to help American med-device companies expedite design, shorten the development cycle and enhance long-term performance. It is our goal to design scalable, compliant and technologically advanced medical products that improve operational workflow and patient care across U.S. hospitals, clinics, laboratories and research facilities.
We handle everything in the development, from concept engineering and feasibility analysis to CAD 3D modeling, prototype creation, testing and certification. Leveraging extensive industry expertise and advanced capabilities in product design, our US customers have access to accelerated prototyping, minimized risk of engineering failure mode errors and scalable solutions designed to thrive in complex clinical environments. Each product that we offer is skillfully constructed and designed to meet the standards with regards to safety, ease of use, and customer satisfaction that are required by America’s healthcare professionals. Our agile development methodology can enable clients to receive faster prototype validation, easier integration into clinical workflows and more rapid time-to-market.
Support doesn’t end there, Aqlix provides maintenance support, technical enhancements, clinical performance monitoring and version upgrades following implementation. This is necessary to keep devices safe, effective and in compliance with shifting healthcare requirements. Our focus is on creating partnerships that provide our customers with ways to compete and grow today, while ensuring continuous support of their needs into the future. With Aqlix as their ally, organizations can trust that they are identifying the right products to bring to market through cutting-edge medical products and achieving cost reductions by quickly getting these items within reach of patients.
Each milestone reflects our passion for purposeful delivery

Top questions about medical product development in the U.S.
Aqlix provides specialized engineering, regulatory and design knowledge to expedite development and assure clinical compliance delivering enhanced usability and operational performance.
We assist hospitals, clinics, biotech companies, medical device manufacturers and research labs with the compliant design of medical products.
Most assignments are 12–24 weeks depending on complexity, integrations and regulation. Our workflows and prototyping accelerate time to market.
Yes. We also provide for the continual updates, optimization, performance monitoring and long-term maintenance of U.S. healthcare compliance.
Absolutely. Our devices integrate with EMR, CRMs, IoT platforms & cloud solutions to enhance clinical and operational experiences.
Yes. All products are built to grow with new features, users and compliance changes without being rewritten at great expense.
With our U.S.-based focus, regulatory accuracy, engineering acumen and track record of success, we are the ideal partner for rapid, safe and scalable development of medical products.