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  1. Center for Devices and Radiological Health

Subscribe to CDRH Mailing Lists

Sign up to receive email updates on these CDRH topics - you may unsubscribe at any time. You can also edit your Email Subscription Settings here.

CDRH New

The previous business-day's new additions to the CDRH website.

CDRH Industry

Email updates for new or updated content that is specifically related to industry.

CDRH Science

Updates on regulatory science, the science of developing new tools, standards and approaches to assess the safety, efficacy, quality, and performance of medical devices and radiation-emitting products.

Consumer Information for Medical Devices

Notifications for consumers about medical device information, recently approved devices, and alerts that may be of interest to the general public.

Digital Health

Get news about digital health products and how the FDA regulates them.

FDA Radiological Health Program

News about radiological products and procedures regulated by FDA, and FDA’s role in radiation safety.

Global UDI Database (GUDID) System Status

Provides email alerts regarding database updates and system status for the Global Unique Device Identification Database.

In Vitro Diagnostics

Updates on in-home and laboratory diagnostic tests including 510(k) decision summaries, guidances, and upcoming meetings.

Lasers

Receive updates pertaining to all forms of lasers.

Mammography

A mailing list that announces new mammography documents and updates on Mammography.

Medical Device Safety and Recalls

Notices on medical device recalls, safety communications, alerts, articles, and other safety information.

Medical Device Single Audit Program (MDSAP)

Email notifications when MDSAP documents are updated.

Medical Product Safety Network (MedSun)

Adverse event reporting program for the clinical community to identify, understand, and solve problems with the use of medical devices.

Private Payor Communication

Receive updates on Private Payor Communication.

Recent Device Approvals

Announces when consumer information is available regarding medical devices that FDA has recently approved.

Unique Device Identification (UDI)

Information on how the use of a Unique Device Identification (UDI) system may improve patient safety.