Trusted by 200+ MedTech teams across the globe

Talk to a Regulatory Expert About Your Device.

Years of regulatory experience
The person on your call, named to you
10–25
To your first answer
From a reviewer, not a form
1 day
FDA decisions in our database
What we check your device against
175,000+
Emboa MedPMS MedikalMedDev StrategiesExodus New VenturesMedLaunchStatera RegEndeavor OrthoMed InstituteMDC AssociatesAvio MedtechNeuster Health

Speak to a regulatory expert

A 30-minute consultation with our team.

No charge, no obligation.

What happens next
  1. You submit
  2. We reach out
  3. Book your call

Frequently asked questions

What happens on the call?

It's an initial consultation. We get to know your device and your regulatory situation, and figure out together whether Complizen is a fit. No slides, no pressure, no commitment.

What if I don't need Complizen?

We'll tell you. If the free device check shows your device is Class I and exempt, or a different pathway fits better, we say so — free, and before you've spent anything.

Is this the same as the free device check?

No. The free check is a two-minute automated read of your product code, class and pathway. This call is a real conversation with a regulatory expert about your specific situation — use either one first, whichever fits how you like to start.

Who should join from my team?

Whoever owns regulatory strategy or the submission itself — RA leads, founders, or consultants. We're happy to run a follow-up call later for engineering, quality, or leadership if they'd like their own walkthrough.

Do I need to share confidential device info?

No. The call uses general examples, so you don't need to bring anything sensitive. If you decide to move forward, anything you do bring in stays on encrypted, SOC 2 aligned infrastructure, and we never use customer data to train AI models.

How fast can my team get started after the call?

Same day, if you're ready. We confirm scope and a fixed price before anything begins — no hourly billing, no surprises.