Arrotek guides medtech startups through design, feasibility, and regulatory complexity, giving you confidence to progress without costly mistakes.
Early-stage medtech teams often move fast but lack clarity on design, feasibility, and regulatory pathways. This creates risk and wasted capital.
Uncertainty on FDA/CE pathway
Risk of wasted spend on the wrong design
Struggle to move from idea to working prototype
Arrotek accelerates your journey from sketch to prototype with a structured process, integrated expertise, and regulatory clarity from day one.
From concept to prototype in 90 to 180 days, with clarity at every step.
Design, engineering, and regulatory aligned in one accountable partner.
Compliance from day one, no costly rework later.
Future-proofed for scale with Ireland, Boston, and Costa Rica capacity.
The Prototype Sprint is a structured, fixed-scope engagement that delivers a manufacturable prototype and regulatory clarity. It gives you momentum and confidence to move forward.
Define User Requirements
Group Ideation
Select Designs
Produce Physical
Models
Select One Design
Based On Refined Design
We embed with your team from the very first conversation, guiding you through a structured process that gives you clarity and momentum.
Understand your concept
Design with compliance in mind
Deliver structured outcomes
Support your next steps
Whether you are a startup or an OEM, Arrotek is ready to help you accelerate development with clarity and compliance built in from day one
