Profound Medical TULSA-PRO System Installations Reach 78
Profound Medical announce that its TULSA-PRO system installed base stood at 78 as of December 31, 2025 - higher than its previously announced goal of 75 installs by the end of 2025. Profound's TULSA-PRO qualified sales pipeline also grew to 97 new systems being classified within one of the "Verify, Negotiate and Contracting" stages at year-end. "As the installed base grows, we expect that it will lead to higher patient treatment rates and, correspondingly, continued growth of our high margin recurring revenue," said Profound's CEO and Chairman, Arun Menawat. "That is being driven primarily by the TULSA Procedure's ability to treat an unrivaled range of prostate diseases, severities, and aggressions, while preserving crucial functions like continence and sexual health of the patient. We look forward to releasing our fourth quarter and full year 2025 financial results near the end of February 2026."
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- Successful First Treatment: Mount Sinai Hospital has successfully performed its first TULSA-PRO® prostate cancer treatment, establishing its leadership in robotic surgical care, with the patient discharged the same day, demonstrating the efficiency and safety of the procedure.
- Technological Innovation: The TULSA Procedure™ employs robotically controlled ultrasound to precisely heat prostate tissue to 55-57°C, ensuring no bleeding or hospital stay while maximizing protection of patient nerves and physiological functions, thereby reducing postoperative side effects.
- Clinical Application Prospects: This technology is applicable not only for prostate cancer patients but also effectively treats benign prostatic hyperplasia (BPH), providing patients with more optimal treatment options and paving the way for future research and guideline development.
- Market Potential: Profound Medical's TULSA-PRO® system is CE marked and FDA 510(k) cleared, expected to become a mainstream treatment option for prostate diseases, addressing the growing market demand.

- Successful Financing: Profound Medical has completed a private placement to Canadian investors, issuing 921,428 common shares at $7 each, raising approximately $6.45 million, which enhances the company's financial strength for future growth.
- Clear Use of Proceeds: The funds will be allocated for sales and marketing expansion, research and development, strategic transactions, and general corporate purposes, indicating the company's commitment to market and technological innovation.
- Compliance Assurance: The securities issued are not registered under U.S. securities laws and are subject to a four-month hold period, ensuring the company operates within a compliant framework to mitigate legal risks.
- Broad Technological Prospects: Profound's TULSA-PRO system and Sonalleve platform show significant potential in the non-invasive treatment sector, with ongoing technological innovation and market expansion expected to enhance the company's competitiveness in the medical device industry.
- Increased Financing Size: Profound Medical Corp. has expanded its private placement to raise $6.45 million by issuing 921,428 common shares at $7 each, reflecting strong interest from long-term investors.
- Clear Use of Proceeds: The net proceeds will be allocated for sales and marketing expansion, research and development, strategic transactions, and general corporate purposes, aimed at enhancing the company's market competitiveness and innovation capabilities.
- Compliance Considerations: The securities offered will not be sold to U.S. purchasers, ensuring compliance with U.S. securities laws and reducing legal risks associated with the offering.
- Optimistic Market Outlook: Profound Medical focuses on developing incision-free treatment technologies, particularly the TULSA-PRO system, which is expected to drive growth in its market share within the prostate disease treatment sector.

- Increased Offering Size: Profound Medical has expanded its private placement to raise $6.45 million by issuing 921,428 common shares at $7 each, accommodating participation from a long-term investor, thereby enhancing liquidity.
- Clear Use of Proceeds: The net proceeds from this offering will be allocated to sales and marketing expansion, research and development, strategic transactions, and general corporate purposes, aiming to strengthen the company's competitive position in the medical device market.
- Compliance Statement: No securities will be sold to U.S. purchasers under this offering, ensuring compliance with U.S. securities laws, which mitigates legal risks and protects the interests of both the company and its investors.
- Technological Background: Profound Medical focuses on developing AI-powered, incision-free therapies, with the TULSA-PRO system poised to become a mainstream treatment option for prostate diseases, enhancing patient quality of life and driving long-term growth for the company.
- Funding Scale: Profound Medical Corp. is raising up to $40 million through a registered direct offering of 5,142,857 common shares at $7 each, demonstrating strong market appeal and investor confidence.
- Use of Proceeds: The funds will be allocated for sales and marketing expansion, research and development, and strategic transactions, aimed at enhancing the company's competitive edge and innovation capabilities to drive future growth.
- Private Placement Plan: The company also plans a private placement of up to 571,428 shares at $7 each to raise an additional $4 million, expected to close by December 30, showcasing flexible capital management.
- Market Reaction: The offering, led by healthcare-focused investors, is anticipated to close on December 22, reflecting strong investor confidence in Profound's future development.

- Honor Recognition: Profound Medical's Dr. Pejman Ghanouni received the Cum Laude award at the 2025 RSNA Annual Meeting for his research on the TULSA procedure, highlighting the company's academic influence in prostate cancer treatment and enhancing its brand reputation.
- Clinical Data Advantage: The TULSA procedure allows patients to return to normal activities the day after treatment, compared to nearly three weeks for traditional robotic prostatectomy patients, significantly improving patient experience and potentially driving market demand.
- CAPTAIN Trial Results: The CAPTAIN trial recruited 210 patients across 20 sites in the U.S. and beyond, with 69% receiving the TULSA procedure, providing robust clinical data that further validates TULSA's safety and efficacy.
- Technological Innovation: The TULSA-PRO system integrates real-time MRI and AI technology to deliver personalized therapy, ensuring precise ablation of prostate tissue, marking a significant advancement in prostate disease treatment that could reshape the industry landscape.






