At Salt Medical, we specialise in transforming early-stage ideas into validated, production-ready prototypes. With deep expertise in minimally invasive devices, we partner with you at every stage, from concept ideation through regulatory-conscious design refinement to prototype realisation.
Medical-device domain expertise — Our engineers understand the unique challenges of minimally invasive devices (biocompatibility, sterilization, miniaturization, regulatory constraints).
End-to-end continuity — Design outputs are optimized for in-house prototyping and downstream manufacturing, minimizing translation losses.
Iterative, risk-aware process — We embed risk analyses, design for manufacturability (DfM), and design for regulatory compliance early.
State-of-the-art tools & environments — Advanced CAD, multiphysics simulation, rapid prototyping labs, and cleanroom integration.
Collaborative, transparent workflow — You stay involved in design decisions via milestones, reviews, and shared access to digital assets.
Proven track record — Decades of experience from the team at Salt Medical, delivering medical device programs with quality, speed, and traceability.
Concept & Feasibility
Preliminary Design
Detail Design & DfM Review
Prototype & Validation
Design Freeze & Handoff
Full CAD models and assemblies
Engineering drawings & tolerancing
Design specification documents & interface control documents
Material selections & justification
Risk assessment (e.g. FMEA), design validation plan
Prototype units (functional, fit/form)
Test reports from in-house or subcontracted labs
Transition package for prototyping or production
At Salt Medical, design development doesn’t end when CAD is complete, we seamlessly transition into prototype realization. Our internal rapid prototyping and partner network ensure your concept is physically tested, validated, and refined before scaling.
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