Innokas has been known as trusted Nordic partner for companies developing medical devices, with end-to-end services across the entire product life cycle, for over thirty decades. We operate under an advanced ISO 13485-based system, ensuring that every customer project meets the highest quality standards. Our team’s capabilities span product design, development, software engineering, fast scaling manufacturing, and quality/regulatory consulting to effectively shorten time-to-market for complex, safety-critical next-gen medical devices.
Innokas team trusts in collaboration, sustainability, and continuous improvement. Adaptable approach and proven processes make us a reliable choice for innovative medical technology companies seeking long-term success.
Quality and regulatory expertise has been at the heart of our medtech operations from the very beginning. We ensure every medical and IVD device meets global standards, from EU MDR to FDA. Our dedicated QA/RA team proactively manages risk and resolves compliance challenges early, preventing costly changes and safeguarding product safety and conformity throughout the development process.
For decades, our medtech engineering team has delivered agile product development for even the most complex medical devices. We turn challenging concepts into manufacturable solutions quickly and efficiently according to any relevant standards. Our developers also continue to give their support to the product even after development has wrapped up and it's time for production. Continuous improvement lies in the readiness to innovate further.
Two locations, endless possibilities. With two dedicated manufacturing sites, we make sure Healthtech innovators get exactly what they need from scalable medical device manufacturing, from fast ramp-up to cost-efficient volume production for steady growth. Both FDA registered factories are rigorously audited to maintain utmost quality standards, so every product leaving our lines is ready to perform.
We don’t believe in walking away when there’s more we can do. From concept to well beyond market entry, we partner with you throughout the entire medical device lifecycle. Keeping your innovative Healthtech solution current is easier with someone who’s been there from the start. Through continuous support and proactive updates, we’ll make sure what you’ve built stands the test of time.
We deliver secure, compliant medical software, including SaMD and embedded systems. Our experts ensure regulatory compliance and safe AI integration. Cybersecurity services include penetration testing, vulnerability scanning, SAST, and automated SBOM with CVE checks to protect sensitive data build resilience. From concept to turnkey implementation, we construct safety-critical solutions that meet the highest standards.
We embed sustainability and circular economy principles across the entire medtech value chain. That means considering circular design principles right from the product development phase and maintaining transparency and traceability throughout production. Our trusted supply chain is closely monitored. Sustainability begins with a step and turns into journey that delivers long-term value for your innovation and future generations.
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