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AIROS Medical Receives FDA Clearance to Market New Peristaltic

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AIROS Medical announces FDA 510k clearance to market the AIROS 8P compression device and Pants garment that treats leg and pelvic swelling.

FDA approves Beyond Air LungFit PH to treat hypoxic respiratory failure

FDA approves LungFit PH to treat respiratory failure in neonates

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Innovative Wound Solutions

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AIROS Medical granted FDA 510k clearance to market compression device for Lymphedema treatment - NS Medical Devices

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AIROS Medical Granted U.S. Trademark Registration for Company, Brand Name

aeri-20201231