Ann: Orthocell Webinar Presentation, page-6

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    Thanks Bedger as always. Here's an AI read that may fill any gaps missed. Excuse the spelling an typesetting it is unedited.

    Company Overview and Recent Developments (04:45 - 09:34)
    Orthocell is an Australian medical device company with growing international revenue
    FDA clearance pending for breakthrough nerve repair device
    Products approved in 9 international jurisdictions
    StriPlus (first product) received FDA clearance, approved in UK, EU, Australia, New Zealand, Canada
    REMPLAR (nerve repair device) approved in Australia, New Zealand, Singapore
    Company manufactures own products, owns manufacturing margin and scientific narrative
    Three consecutive quarters of record revenue, reporting 2.2 million in December quarter

    Board Changes and Financial Position (09:35 - 13:51)
    Complete board change in last two years
    New chair: John van der Willen
    Dr. Ravi Thotani: Former Harvard Medical School professor, FDA consultant
    Hon. Kim Beazley: Geopolitical and defence knowledge
    Prof. Fiona Wood: Ex-Australian of the Year, plastic reconstructive surgeon
    Strong balance sheet: $32 million in bank, no debt, no royalties
    Growing interest from institutional investors

    Product Portfolio and Manufacturing (13:52 - 17:53)
    First product: StriPlus (bone repair), partnered with BioHorizons
    Second product: REMPLAR (nerve repair)
    Third product: Smart Graft (tendon repair), submitted for TGA approval
    Unique manufacturing process producing pure, decellularized collagen
    Over 70,000 implantations internationally

    REMPLAR Technology and Market Potential (17:54 - 23:33)
    REMPLAR redefining nerve repair, mimics nerve's epineurium
    Reduces or negates use of sutures, improves clinical outcomes
    Three indications: connect, protect, and cap nerves
    85% recovery rate in clinical data
    Over 180 surgeons in 130+ hospitals using REMPLAR in Australia
    700,000+ peripheral nerve repairs performed annually in US

    US Market Entry and Global Expansion (23:34 - 31:12)
    FDA 510k clearance expected late March/early April
    Appointed two US-based executives with Axogen experience
    Building US team, engaging distributors, establishing key accounts
    Expanding global footprint: submissions in Canada, Thailand, EU, UK, Brazil
    $3.5 billion total addressable market
    Aiming for 20% market share
    Strong commercial phase with validated products and strong balance sheet
 
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