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Subscribe to CDRH Mailing Lists

Sign up to receive email updates on CDRH topics. Our free email alert service allows you to receive important news and information as they become available. Your email will only be used to deliver the requested information or to give you access to your subscription preferences. Visit FDA’s privacy policy for more details.

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CDRH New

A daily digest of the previous business-day's new additions and updates to CDRH's webpages.

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.

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.

Industry

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

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 Payer Communication

Receive updates on Private Payor Communication.

Radiological Health Program

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

Recent Device Approvals

A digest email of consumer information about recently approved medical devices.

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.

Unique Device Identification (UDI)

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

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