FOR Designation Could Limit U.S. Investors in Anteris’ Latest Offer
Anteris Technologies has updated the timetable for its Australian capital raising, delaying settlement to November 4 and the start of trading for new securities to November 5. The company also highlights restrictions on U.S. investors acquiring its CDIs.
- Settlement of Australian Offer moved to November 4, 2025
- New CDIs and CDI Warrants to commence trading on ASX November 5, 2025
- FOR designation restricts U.S. persons from acquiring CDIs
- Timetable remains indicative and subject to ASX approval
- Anteris focuses on structural heart medical devices with patented ADAPT tissue technology
Updated Capital Raising Timeline
Anteris Technologies Global Corp., a leader in structural heart medical devices, has announced a revision to the timetable for the Australian component of its ongoing capital raising. The settlement date for the offer has been pushed back by one day to November 4, 2025, with the allotment and commencement of trading for new CHESS Depositary Interests (CDIs) and CDI Warrants now scheduled for November 5, 2025. This adjustment follows the initial announcement made on October 28, 2025.
Implications of the FOR Designation
Alongside the timetable update, Anteris reiterated that the Foreign Ownership Restriction (FOR) designation will apply to all new CDIs. This regulatory measure restricts U.S. persons, as defined under U.S. securities law, from acquiring these securities. The FOR designation aims to ensure compliance with cross-border investment rules but may influence the liquidity and investor base for the new shares on the ASX.
Company and Product Context
Founded in Australia with a significant presence in the United States and Europe, Anteris Technologies is focused on innovative solutions for structural heart disease. Its flagship product, the DurAVR Transcatheter Heart Valve, is a biomimetic device designed to replicate the function of a healthy aortic valve. The valve incorporates Anteris’ patented ADAPT tissue technology, which has FDA clearance and a decade-long clinical track record in over 55,000 patients worldwide.
Market and Regulatory Considerations
The updated timetable remains indicative and subject to change at the company’s discretion, pending ASX approval. Investors should note that such adjustments are not uncommon in capital raising processes but can affect trading strategies and market sentiment. The FOR designation, while regulatory in nature, introduces an additional layer of complexity for U.S.-based investors and may impact demand dynamics for the new securities.
Looking Ahead
As Anteris progresses with this capital raising, market participants will be watching closely for final ASX approvals and any further timetable changes. The company’s ability to successfully complete this raise will be critical in supporting its ongoing development and commercialization efforts in the competitive structural heart device sector.
Bottom Line?
Anteris’ revised timetable and regulatory restrictions set the stage for a closely watched capital raise with potential market implications.
Questions in the middle?
- How will the FOR designation impact liquidity and investor participation on the ASX?
- What are the potential uses of the capital raised in this offering?
- Could further timetable changes affect investor confidence or share price momentum?