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The Over-the-Counter Hearing Aid Act of 2017 (OTC Hearing Aid Act) was a law passed by the 115th United States Congress as a rider on the FDA Reauthorization Act of 2017. It created a class of hearing aids regulated by the Food and Drug Administration (FDA) available directly to consumers without involvement from a licensed professional (like an audiologist, otolaryngologist, or audiometrist). [1]
A BBB-accredited company agrees to abide by a set of accreditation standards BBB says are "attributes of a better business." These include honesty in advertising, transparency, and responsiveness ...
Given that hearing loss has implications in everything from diabetes to heart health to the risk of falling, experts said catching it early can have profound quality-of-life implications.
The hearing aid market has advanced by leaps and bounds since the FDA's 2022 regulatory change allowing hearing aids to be sold over the counter. The greatly increased competition between ...
Hearing aids are used for a variety of pathologies including sensorineural hearing loss, conductive hearing loss, and single-sided deafness. Hearing aid candidacy was traditionally determined by a Doctor of Audiology, or a certified hearing specialist, who will also fit the device based on the nature and degree of the hearing loss being treated.
The FDA will allow hearing aids to be purchased over-the-counter for people 18 or older with mild to moderate hearing impairment as early as October.