Investor Presentaiton

IMDRF International Medical Device Regulators Forum MEDICAL DEVICE SAFETY ACTION PLAN: PROTECTING PATIENTS, PROMOTING PUBLIC HEALTH 1. Establish a robust medical device patient safety net in the United States 2. Explore regulatory options to streamline and modernize timely implementation of postmarket mitigations 3. Spur innovation towards safer medical devices 4. Advance medical device cybersecurity 5. Integrate the Center for Devices and Radiological Health's premarket and postmarket offices and activities to advance the use of a TPLC approach to device safety https://www.fda.gov/downloads/AboutFDA/Centers Offices/OfficeofMedical Productsand Tobacco/CDRH/CDRHReports/UCM604690.pdf 2

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