Advanced solutions
Revolutionary product
Invest in the future of
cardiac care
Join us in transforming cardiac procedures with innovative technology designed for safety and efficiency.
Investment opportunity
Invest in the future with ArchCath
"The global transcatheter heart valve replacement (TAVR) market is worth US$ 5.7 Billion for 2022, and is set to expand 4.0X over the next ten years."
Why Invest?
The GateKeeper® Catheter market potential
Expanding global market
The global TAVR market is projected to reach USD 8 billion by 2025, driven by an aging population and increasing preference for minimally invasive surgeries.
Increasing demand
Technological advancement
Regulatory support
Regulatory support
Insurance and reimbursement
Expanding insurance coverage for TAVR procedures and associated protective technologies ensures broader market accessibility and adoption.
Long-term cost savings
Reducing complications such as strokes in TAVR procedures can lead to significant long-term cost savings for healthcare systems worldwide.
Scalability potential
Connect with our team
For more detailed information and to discuss potential investment opportunities, please contact our Investor Relations team. We are ready to support you in making an informed investment decision and welcome you to the ArchCath family.
For Investors
Investing in GateKeeper® Catheter
Market Pontential
Capitalize on the expanding market for TAVR procedures and stroke prevention technologies
Innovation and Growth
Be part of pioneering journey with a product backed by robust patents and proven market demand
Market Pontential
Capitalize on the expanding market for TAVR procedures and stroke prevention technologies
Innovation and Growth
Be part of pioneering journey with a product backed by robust patents and proven market demand
Timeline
Milestones and achievements
2016
Company formation and first US patent issuance.
2019
Successful prototype development and proof-of-concept animal trials.
2021
FDA 510(k) clearance received, enabling clinical application.
2021
First-in-human testing demonstrated safety and efficacy.
2022 - 2024
Ongoing clinical studies and preparation for pivotal trials.