From early design reviews to vendor collaboration, our medical device engineering services are built to get it right from the start. We consult on material selection, 3D drawing services, and mold flow analysis, solving design challenges before they hit the mold.
We help refine mold tooling designs to improve flow, gating, and part release, reducing cycle times, increasing quality, and preventing rework.
We help match your part to the right resin, balancing strength, flexibility, chemical resistance, and regulatory needs for your application.
Our engineers use 3D drawing services and mold flow analysis to flag draft angles, wall thickness, and gating concerns to avoid costly design errors.
As a privately owned company, we move fast, pivot when needed, and prioritize what matters. Our engineers adapt to evolving needs, helping OEMs solve design challenges without slowing progress.
Our medical device engineering services blend real-world tooling expertise with advanced consultation to support complex geometries, tight tolerances, and Class I–III requirements. From Design for Manufacturability (DFM) to mold flow analysis, resin selection, and secondary process planning, we help OEMs design smarter, scale faster, and reduce risk—long before the first shot.
We consult early to flag geometry, gating, and tolerance issues, solving design problems before they hit tooling, reducing late changes and added development costs.
Mold flow analysis lets us identify risks like warpage and air traps, helping optimize gating, wall thickness, and cooling strategies—before tooling investment is made.
We guide resin selection based on strength, flexibility, chemical resistance, and regulatory needs, factoring in downstream assembly, labeling, and sterilization.
Medical device engineering ensures your part is moldable, cleanroom-compatible, and ready for production, aligned with ISO 13485 and downstream compliance.
Our medical device engineering services support components across Class I, II, and III programs—guided by deep manufacturing insight, regulatory experience, and cleanroom compatibility. Whether you're designing for injection molding, automation, or downstream validation, we help ensure your product is optimized for compliance, scale, and production success.
We offer injection molding and injection blow molding—optimized for precision, compliance, and scale in cleanroom environments.
We operate an 8,000 sq. ft. ISO Class 8 cleanroom with injection molding and injection blow molding, built for high-quality, compliant component production.
From manual to automated assembly in our white room and cleanroom, we deliver finished components with precision, speed, and traceability.
We help OEMs bring complex molded components to life—with the care, speed, and flexibility they depend on.
We serve a variety of markets, and our medical device engineering services go beyond design checks. We bring hands-on manufacturing insight to help OEMs avoid downstream issues and make smarter decisions early. Whether it’s material selection, mold flow analysis, or tooling guidance, we focus on practical, production-ready outcomes—and work with you to get it done right.
The earlier the better. Involving us during concept development or design refinement allows our medical device engineering team to identify manufacturability risks, guide resin selection, and provide input on geometry, gating, and secondary processes—reducing delays and costly design changes.
That’s where we come in. If a design isn’t optimized for molding, performance, or cleanroom compatibility, our engineers offer practical improvements that preserve functionality and reduce production risk, making your part easier and more cost-effective to manufacture.
We help OEMs bring ideas to life—from early concepts to mold-ready parts—applying DFM to streamline tooling and support scalable production.
From IQ through PQ, we validate molding and assembly processes to ensure quality, compliance, and confidence in regulated device production.
