ExThera Medical Corporation

Industry
Medical Device
Founded Year
2007
Headquarters
757 Arnold Dr Ste B, Martinez, California, 94553, United States
Employee Count
27

Key People


Assessment

Team
Aspect: Multiple successful MedTech entrepreneurs
Summary: The leadership team comprises experienced professionals with backgrounds in medical device development and commercialization.

Robert Ward, serving as President and CEO, brings significant expertise in the medical device sector. The presence of multiple seasoned professionals in key roles suggests a strong foundation for strategic decision-making and product development.

Clinical Need
Aspect: Very Strong
Summary: ExThera Medical addresses critical unmet needs in treating severe bloodstream infections.

The Seraph 100 Microbind Affinity Blood Filter is designed to remove a broad range of pathogens from the bloodstream, offering a novel solution for conditions like sepsis and COVID-19. This innovation meets a significant clinical demand for effective treatments in these areas.

Competition
Aspect: First mover
Summary: ExThera Medical appears to be a pioneer in extracorporeal blood filtration for pathogen removal.

As an innovator in this space, ExThera Medical has the advantage of setting industry standards but may also face hurdles in educating the market and establishing trust in new treatment modalities.

Technical Challenge
Aspect: Predictable
Summary: The technology involves established principles of blood filtration and pathogen removal.

Utilizing adsorption techniques to remove pathogens from the bloodstream is a concept grounded in existing medical knowledge, suggesting a manageable path through technical development and regulatory approval.

Patent
Aspect: Very Strong
Summary: ExThera Medical holds robust intellectual property rights for its technologies.

The company's patents cover key aspects of its blood filtration devices, providing a barrier to entry for competitors and securing its market position.

Financing
Aspect: Well-funded
Summary: The company has secured substantial funding to support its operations and growth.

With total funding of approximately $54.6 million from multiple investors, ExThera Medical has the financial resources necessary to advance its product pipeline and commercial strategies.

Regulatory
Aspect: 510k/PMA
Summary: The Seraph 100 has obtained CE Mark and FDA Emergency Use Authorization.

Achieving CE Mark certification in the EU and FDA EUA in the U.S. demonstrates compliance with stringent regulatory standards, enabling the company to market its products in key regions.

Opportunity Rollup

Odds of Success
3.2
Peak Market Share
3.75
Segment CAGR
5.4%
Market Segment
Medical Devices
Market Sub Segment
Bloodstream Infection Treatment Devices
Year Post Launch Market Penetration (%)
1 0.19
2 0.56
3 1.31
4 2.62
5 3.75

Key Takeaway

ExThera Medical is well-positioned to address critical needs in bloodstream infection treatment with its innovative Seraph 100 device, supported by a strong team and substantial funding.