Sequence Group

Medical Device Consulting

Welcome to Sequence Group, where we specialize in providing expert guidance and support in the area of device regulatory consulting and medical device design and development.

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Device Consulting

Navigating regulatory challenges are at the heart of our approach. We bring decades of expertise to every engagement, helping medical device companies bring safe, effective products to market.

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QUALIFIED SPECIALISTS

Experienced in all areas of device design and development, from device inception to regulatory submission.

INDIVIDUAL APPROACH

Our consultants are experienced in all aspects of the development life cycle and can guide you through.

GREAT EXPERIENCE

We work with each client individually to ensure the project goals are met and the objectives are achieved.

FRIENDLY CUSTOMER SERVICE

We take the complexity and headache out of the design process. Contact us today to see what we can do for you.

What we do

Market Research

We help you evaluate your device and with market research and determine the appropriate pathway forward.

Project Planning

We bring a straight forward approach to the development planning process to help ensure your project is a success.

Development Lifecycle

We can guide you through each step of the process, including final device preparation and submission.

Regulatory Consulting

Full consulting and guidance is offered through the entire regulatory submission process, including 510k and EU MDR.

Post Market

In addition to guidance on the development process, we provide post market support to help ensure your organization stays compliant.

Proven Strategy

Take the guess work out of the design process and follow our proven development steps to ensure your device makes it to market.

US Agent Services

Foreign manufacturers must designate a US Agent for FDA registration. Sequence Group serves as your official FDA-designated US Agent, handling all correspondence and compliance.

20+ years of experience

50+
Ongoing Projects
200+
Finished Cases
150+
Satisfied Customers
15+
Consultants Worldwide
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Completed Cases

TVM Balloon Applicator

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QMS Overview

Management of Generation Changes

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Sculptura IORT Device

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Treatment Planning System

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GentleBeam™

Image-Guided Superficial Radiation Therapy System

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What our clients say

Sequence Group performed the full software validation on our QMS and helped bridge the gap to bring us to the next level.

M
Melissa Curt
CTO

Thanks to Sequence Group, we were able to develop our Design History File that helped us launch a successful product.

A
Amanda Black
COO

Sequence Group's regulatory consulting guidance was a tremendous help during the initial growth phase of our organization.

L
Larry Johnson
Founder

Sequence Group was vital in providing guidance and support during the design and development process.

D
David S. Thomas
Director of R&D

Latest Posts

EU Regulatory
EU Regulatory

Preparing an EU MDR 2017/745 Submission

A comprehensive guide to preparing your EU MDR 2017/745 submission, covering key requirements and documentation needed f...

Jan 15, 2024Read More →
EU Regulatory
EU Regulatory

The EU MDR 2017/745

Understanding the EU Medical Device Regulation 2017/745 and what it means for your medical device business in the Europe...

Jan 10, 2024Read More →
US Regulatory
US Regulatory

Submitting a 510(k) De Novo to the FDA

Step-by-step guidance on submitting a 510(k) De Novo request to the FDA, including key considerations and documentation ...

Jan 5, 2024Read More →
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We provide solutions to the design process

Take the guess work out of the process and consult with us for a proven pathway forward.

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