Medbio & SBE Case Study - Full Service US Based Cost Effective Partners
In a landscape where many contract manufacturers excel at only one or two aspects of medical device production, MedBio differentiates itself by integrating design, engineering, and manufacturing into a unified, cost-optimized process. Rather than handing projects off between multiple vendors—each adding cost, delay, and variability—MedBio focuses on end-to-end solutions that keep production close to home and tightly controlled.
A key strength lies in early-stage collaboration and design for manufacturability (DFM). MedBio engineers work closely with customers to identify opportunities to simplify geometry, improve material selection, optimize tooling, and streamline assembly. This upstream involvement reduces downstream inefficiencies and ultimately lowers cost of goods sold while improving product reliability and manufacturability.
A real-world example includes the development of an external female urinary collection device aimed at improving patient dignity, reducing hospital-acquired infections, and addressing a critical gap in care. Through iterative design improvements—such as adding pull tabs for easier removal, refining material durometer, and optimizing surface texturing for both adhesion and release—MedBio helped transform an early concept into a manufacturable, scalable product.
The team also leveraged tooling strategies such as thermal management optimization and process refinement through mold flow analysis and structured molding validation. These efforts ensured consistent part integrity while maintaining efficiency in high-volume production.
For startups in particular, MedBio’s engineering support becomes an extension of their internal team, enabling access to deep manufacturing expertise without requiring in-house resources. The result is a streamlined path from concept to commercialized product, with reduced risk, controlled costs, and accelerated time to market—all anchored by a collaborative, problem-solving approach focused on patient impact and real-world usability.
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