Neuromod raises €30m to fund drive into US market
Company’s Lenire device approved by FDA uses sound and electric stimulation to ease symptoms of tinnitus
Source: irishtimes.com
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Company’s Lenire device approved by FDA uses sound and electric stimulation to ease symptoms of tinnitus
Neuromod Devices announced today that it closed a $33.2 million (€30 million) financing round to support its tinnitus treatment device.
Neuromod Devices' non-invasive device, Lenire, is the first of its kind granted approval to treat tinnitus in the US market. At least 25,000,000 Americans are...