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Medical Devices; Ear, Nose, and Throat Devices; Establishing Over-the-Counter Hearing Aids

FR Abstract
The Food and Drug Administration (FDA, we, or the Agency) is establishing a regulatory category for over-the-counter (OTC) hearing aids and making related amendments to update the regulatory framework for hearing aids. Specifically, we define OTC hearing aids and establish applicable requirements; amend existing rules for consistency with the new OTC category; repeal the conditions for sale applicable to hearing aids; amend the existing labeling requirements for hearing aids; and update regulations relating to decisions on applications for exemption from Federal preemption that will become obsolete as a result of changes to the hearing aid requirements. In creating a regulatory category for OTC hearing aids and amending existing rules, we intend to provide reasonable assurance of safety and effectiveness for these devices as well as foster access to, and innovation in, hearing aid technology, thereby protecting and promoting the public health.
Incorporation
FR Document Number
2022-17230
Federal Register Volume
87
Federal Register Year
2022-08-17
Federal Register Start Page
50698
Federal Register End Page
50762
CFR Citation
21 CFR 874
FR Citation
87 FR 50698
CFR title
21
CFR Part
874
Document Number
ANSI ASA S3.22-2014 (R2020)
Document Edition
2014
Standard Title
Specification Of Hearing Aid Characteristics, June 5, 2020
Excerpts
device on or after October 17, 2022. Incorporation by reference: The incorporation by reference of certain material listed in this rule is approved … topics in the sections that follow. D. Incorporation by Reference FDA is incorporating by reference ANSI/CTA-2051, “Personal Sound Amplification Performance … under the incorporation by reference regulations issued by the Office of the Federal Register , incorporation by reference of a publication is limited
Record Source
www.federalregister.gov