Growing Customer Demand for Low-Volumes of Custom Designed Medical Devices
CARLSBAD, Calif., March 9, 2019—Symbient Product Development, a medical product development company that specializes in medical and life science disposables today announced that they increased molding capacity with the addition of a 66-ton Arburg Horizontal Electric injection molding machine. In-house injection molding is a key benefit to Symbient’s product design services, enabling thorough testing of production quality devices that are in development. Combined with the existing 35-ton horizontal and 55-ton vertical Arburg machines, Symbient can now better keep pace with rapidly growing demand for hundreds to low thousands of assemblies needed for clinical trials and testing. Symbient’s proprietary prototype mold design offers many advantages over the traditional aluminum prototype molds. “We can replicate production quality in most cases so that we are not fighting artifacts of typical prototyping molding process.” CEO Scott Castanon stated. “Our engineers, machinists and molding technicians are all in the same building, which gives us a big advantage in communication, improving the speed of development and quality of prototypes” added Castanon. Rapid design of medical products has always been the focus of Symbient Product Development, and the new Arburg 66-ton horizontal machine demonstrates this commitment to meeting our customers’ needs.
About Symbient Product Development
Symbient Product Development specializes in design engineering and design-for-manufacturing of innovative medical and life science devices that use plastics. Our highly experienced team consists of mechanical and biomedical engineers, industrial design talent, machinists and molding technicians. They leverage our in-house rapid prototyping, prototype tooling fabrication and injection molding to create proven, manufacturable designs with unmatched speed, efficiency and quality. These designs form our deep portfolio of over 300 successful devices that have generated hundreds of millions of dollars for our clients. They include FDA Class I, II and III devices, developed under our ISO 13485 certified quality management system.