The smartest way to tackle medical device development is through a phased approach.
For a med device startup founder, the successful transition from "napkin sketch" to "market launch" is the goal, but the financial roadmap must be defined. You need to raise capital, but you can't raise capital without a budget.
At Kapstone Medical, we regularly get this question. Recently, I sat down with Director of Engineering David Considine and CEO & Founder John Kapitan to break down the numbers.
Below is a breakdown of the real-world costs of bringing a device to the US market and the variables that drive them.
5 Factors That Inflate Development Costs
Before looking at the sticker price, you must understand the "drivers." If your device is highly novel, costs increase. If your supply chain is fragile, timelines extend. According to David, these are the five critical variables:
Estimated Costs by FDA Device Classification
To give you a realistic "ballpark," we have categorized costs by FDA risk classification. These estimates assume a "start from scratch" scenario including labor, materials, and standard testing.
(Note: These figures exclude marketing launch costs and large-scale production runs.)
|
FDA Classification |
Complexity |
Est. Cost to Market |
Est. Timeline |
|
Class I |
Low Risk (Non-GMP exempt) |
$100,000-500,000 |
~12 Months |
|
Class II |
Moderate Risk (510(k) Required) |
$500,000 – $1M+ |
18–24 Months |
|
Class III |
High Risk (PMA / Clinicals) |
$1.5M – $5M+ |
3–5 Years |
For a Class II device, which is common for many startups, you are looking at $500k as a baseline. However, if clinical data is required to prove substantial equivalence, that number can easily run north of seven figures.
How to Manage Costs: The Phased Approach
If these numbers look daunting, don't panic. You rarely need 100% of the capital on Day 1.
The smartest way to tackle medical device development is through a Phased Approach.
While we would ideally have all funding guaranteed upfront, we break the process into 'bite-sized' phases. This minimizes risk for the founder and allows you to validate the technology before moving to the next investment tier.
By partitioning the project (e.g., Phase 1: Feasibility, Phase 2: Design Controls), you can use early wins to secure the next round of investment.
Next Steps for Your Project
It is impossible to nail down an exact timeline and cost without a deep dive into your specific technology. However, understanding your FDA classification and partnering with a team that has navigated these waters for decades is the best way to de-risk your launch.
As a single-source solution for taking medical devices from concept through commercialization, Kapstone is the go-to for comprehensive strategies and solutions. Learn more in the Kapstone Medical New Product Development (NPD) Roadmap.