Requests that the FDA create a database of all labels, labeling, and instructions for use (collectively “device labels”) of FDA-regulated medical devices. | Federal Regulations · Congress.wiki

Nonrulemaking

FDA

Open for Comments

FDA-2026-P-0777

Requests that the FDA create a database of all labels, labeling, and instructions for use (collectively “device labels”) of FDA-regulated medical devices.

Documents

Comments

Key Dates

Comment Period OpensJan 28, 2026

Documents

Type	Title	Posted	Comments	Status
Other	Interim Response	Jul 21, 2026	--

Keywords

CDRH

Citizen Petition

Harmed Americans

for Reform in Medical-Device Safety Corp

create a database of all labels

labeling and instructions for use

collectively device labels

of FDA-regulated medical devices

Data from Regulations.gov