Medical Device Servicing Safety and Accountability Act
Official title: To amend the Federal Food, Drug, and Cosmetic Act to require the registration of establishments that service devices, and for other purposes.
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Referred to the Subcommittee on Health.
Medical Device Servicing Safety and Accountability Act
This bill amends the Federal Food, Drug, and Cosmetic Act to require establishments servicing medical devices to register with the Food and Drug Administration (FDA). Such establishments must maintain records and make reports as the FDA requires to ensure the safety and effectiveness of serviced devices.
The bill exempts certain medical facilities, including physician's offices, that service medical devices in accordance with state and local laws.- Introduced in House Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). H.R. 2118: Medical Device Servicing Safety and Accountability Act. 115th Congress. Open America. https://openamerica.io/bill/115-HR-2118/
"H.R. 2118: Medical Device Servicing Safety and Accountability Act." 115th Congress, 2026, Open America, https://openamerica.io/bill/115-HR-2118/.
H.R. 2118, 115th Cong. (2026), https://openamerica.io/bill/115-HR-2118/.
[H.R. 2118: Medical Device Servicing Safety and Accountability Act](https://openamerica.io/bill/115-HR-2118/)