Avisi Technologies’ investigational device exemption for VisiPlate approved by FDA
Key Takeaways VisiPlate’s IDE approval allows clinical studies in the US, focusing on safety and effectiveness data collection for the novel glaucoma treatment device. The device’s unique metamaterial and multichannel design aim to reduce IOP and minimize blockage risks, offering potential advantages over current surgical treatments. VITA trial results demonstrated a 40.4% mean IOP reduction […]