Exterior view of StarFish Medical Toronto office sign on a gray building facade with a brick wall and window in the background.

Toronto – StarFish Medical

Medical Device Design & Engineering – Toronto

Full-service product development for innovative MedTech companies

Complete medical device design, engineering, and manufacturing support from the heart of Canada’s largest life sciences hub.

Housed in the historic Benjamin Moore building in the Junction, our facility brings together cross-functional teams dedicated to transforming complex ideas into manufacturable, regulatory-ready medical technologies.

Expert Medical Device Development in Toronto

Our Toronto-based team of engineers, designers, and commercialization specialists supports every stage of the medical device lifecycle:

Group of professionals at StarFish Medical Toronto reviewing prototypes and discussing medical device design concepts.

Medical Device Design & Systems Engineering

We integrate mechanical, electrical, firmware, software, and optical systems into unified device architectures that balance technical feasibility, regulatory requirements, and business goals.

Hands applying a wearable medical sensor prototype to a patient’s wrist during testing.

Human Factors Engineering & Industrial Design

Our usability experts ensure medical devices are intuitive, safe, and compliant with global standards through rigorous human factors research and user-centered design.

Team members collaborating at a whiteboard covered with sticky notes during a design session in Toronto.

Design for Manufacturing (DFM)

Our team identifies risks early and develops robust processes that enable cost-effective, scalable manufacturing without sacrificing performance or compliance.

Engineer reviewing design documents at a workstation in the Toronto office.

Regulatory Strategy & Quality Systems

We support FDA, Health Canada, EU MDR, and other global submissions with regulatory strategies tailored to each device class and clinical application.

Engineer operating specialized lab equipment inside StarFish Medical Toronto office.

Medical Device Manufacturing & Transfer to Production

We guide clients through pilot builds, documentation packages, verification and validation (V&V), and smooth handoffs to in-house or contract manufacturers.

Team of engineers at StarFish Medical Toronto collaborating during a design review meeting with prototypes on the table.

Commercialization Support

StarFish Medical helps MedTech companies bridge the gap between product development and commercial success, supporting business planning, IP strategy, and fundraising preparation.

Precision optics and laser alignment equipment used in medical device development at Toronto facility.

Specialized Sectors We Serve

Our Toronto office contributes to projects across a broad spectrum of clinical and technological domains, including:

  • Digital health & wearables
  • Diagnostics & imaging
  • Therapeutic devices
  • Surgical & acute care technologies
  • Ophthalmology, cardiology, and orthopedics

Anchored in Toronto’s Life Sciences Ecosystem

We actively collaborate with leading organizations in the region, including:

  • MaRS Discovery District
  • OBIO (Ontario Bioscience Innovation Organization)
Toronto skyline featuring the CN Tower and waterfront on a clear day.
Close-up of a golden location pin marker on a city map, symbolizing StarFish Medical Toronto’s location.

Toronto as a Medtech Innovation Hub

Toronto is home to one of North America’s most active medical technology ecosystems. Our team is deeply embedded in this landscape, offering clients access to a network of clinical collaborators, pilot production partners, and regulatory advisors.

Frequently Asked Questions

What types of medical devices do you develop in Toronto?

We support Class I–III systems, wearables, diagnostics, therapeutic tools, and surgical platforms.

Do you offer medical device manufacturing in Toronto?

Yes — including pilot builds, documentation, and design transfer to CMOs.

Can you help with FDA and Health Canada submissions?

Yes — we provide fully integrated regulatory support for Canadian and U.S. markets.

What sets your Toronto medtech team apart?

Multidisciplinary expertise, ISO 13485-certified processes, and strong local partnerships.

Nick showing a biofilm conference book while Nigel listens, with overlay text reading FDA Asked For It and a red arrow pointing to the book.

When reviewing evidence for a medical device, a single citation can shape an entire submission. In this Bio Break episode, Nick shares a biofilm referencing lesson that has stayed with him since the early 2000s.

Diagram showing medical device at the center connected to clinicians, patients, and regulatory bodies with text 'Who are we designing for?' highlighting stakeholder mapping in MedTech design.

Every phase of a device’s life cycle involves different people with distinct needs—from clinicians and patients to service technicians and regulatory bodies.

A fluorescent protein assay sample glows under UV light as part of medical device cleaning validation testing.

Nick Allan and Nigel Syrotuck explain how a fluorescent protein assay helps engineers measure contamination and cleaning performance in medical devices.