Related Experiment Video
Updated: Mar 10, 2026

Author Spotlight: Methodologies and Advancements of Chronic Pain Management Research
Published on: January 5, 2024
FDA Regulation of Neurological and Physical Medicine Devices: Access to Safe and Effective Neurotechnologies for All
Leigh Anderson1, Patrick Antkowiak1, Aden Asefa1
1Division of Neurological and Physical Medicine Devices, Office of Device Evaluation, Center for Devices and Radiological Health, United States Food and Drug Administration, Room 2680, Building 66, 10903 New Hampshire Avenue, Silver Spring, MD 20993, USA.
Abstract:
The United States Food and Drug Administration (FDA) ensures that patients in the U.S. have access to safe and effective medical devices. The Division of Neurological and Physical Medicine Devices reviews medical technologies that interface with the nervous system. This article addresses how to navigate the FDA's regulatory landscape to successfully bring medical devices to patients.
More Related Videos
Related Concept Videos
Drug Regulation
FDA Approved Drugs: Changes to Approved Drugs
Drug Control Governance: Regulatory Bodies and Their Impact
Impact of Pharmacokinetic–Pharmacodynamic Models: Regulatory Decisions
The Blood-brain Barrier
Neural Regulation

