It took 1.5 years. The submission date was August 2021.Does anyone know when Neuromod applied for FDA approval? Did it take a year or so for Lenire to be approved?
It has been categorized as De Novo class II device. One of the risks stated was an increase in tinnitus. Mitigation for this was clinical performance testing and labeling the device/warning. There was also a side effect of hearing loss due to overstimulation.
Just wow. I don't think the FDA knows the impact of a tinnitus increase on a human being.
Here is some information from the FDA directly on the De Novo classification for Lenire and the assessment and approval. Fun read.
https://www.accessdata.fda.gov/cdrh_docs/pdf21/DEN210033.pdf