Full Spectrum Software has been the go-to software partner for many world-leading medical device companies for over two decades. Not very many companies can boast the breadth and depth of expertise Full Spectrum has in this field. With a background of over 450 products, including many Class III devices, Full Spectrum can help you build a quality product you can count on!
Software development at Full Spectrum Software follows a mature Quality Management System (QMS) built per ISO 13485:2016 standards and adheres to IEC and federal regulations, including but not limited to, 14971, 60601, 62304, HE75, CFR 820.30, and HIPAA. Many of our products have received FDA approval within record times. We have also developed many Class I and Class II devices and understand not all products have the same level of regulatory requirements. We will develop a customized approach that best serves your needs. We often work with many clients to develop Prototypes and Minimum Viable Products (MVPs) in both regulatory and non-regulatory environments.
When choosing a software development partner, it’s important to choose a company that values the affect the products have on people’s lives. We take great pride in developing products that are ultimately helpful for everyone’s well-being. Full Spectrum’s dedication to produce the highest quality products is evidenced by our values. With a senior level engineering team committed to developing high-quality software for complex medical devices, you can be assured of a product you can rely on.
Our portfolio includes a wide variety of products in: