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Subscribe to CDRH Mailing Lists

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New ItemsSent out each business day. Contains a list and links to items added to the CDRH website on the previous business day.(Subscribe)
Breast-ImplantsInformation about upcoming events, panel meetings, and safety information associated with breast implants.(Subscribe)
CDRH ScienceUpdates 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.(Subscribe)
CDRH TransparencyIn support of the FDA Transparency Initiative, CDRH is providing additional information to help the public understand its processes and decisions.(Subscribe)
Contact Lenses Contact lens safety news and information about the latest innovations in contact lenses.(Subscribe)
eMDR – electronic Medical Device ReportingThe electronic Medical Device Reporting (eMDR) project provides the capability for electronic data entry and processing of medical device adverse event reports.(Subscribe)
Event Problem CodesUpdates on enhanced device and patient problem codes that will be going live July 1, 2009. The FDA has provided this information in advance to help you familiarize yourselves with Event Problem Code updates BEFORE the new codes "go live" and are accepted in MAUDE.(Subscribe)
FDA Patient Safety NewsThis mailing list notifies subscribers when new programs in the FDA Patient Safety News series are available for viewing. FDA Patient Safety News is a televised series for health care personnel featuring information on new drugs, biologics and medical devices, on FDA safety notifications and product recalls, and on ways to protect patients when using medical products.(Subscribe)
FDA Radiological Health ProgramNews about radiological products and procedures regulated by FDA, and FDA’s role in radiation safety.(Subscribe)
MammographyA mailing list that announces new mammography documents and updates to the CDRH/Mammography Web Site.(Subscribe)
Medical Device Epidemiology Network InitiativeMailing list for the Medical Device Epidemiology Network Initiative (MDEpiNet), a collaborative program through which CDRH and external partners share information and resources to enhance our understanding of the safety and effectiveness of medical devices after they are marketed.(Subscribe)
Medical Device RecallsNotices about Class I medical device recalls and some Class II and III recalls of interest to consumers.(Subscribe)
Medical Device Safety Updates for health care professionals on device recalls, Public Health Notifications, and other safety information.(Subscribe)
MedSun – Medical Product Safety NetworkThe Medical Product Safety Network (MedSun) improves FDA’s understanding of problems with the use of medical devices so that the FDA, healthcare facilities, clinicians, and manufacturers can better address safety concerns.(Subscribe)
Office of In Vitro DiagnosticsUpdates on 510(k) decision summaries, Turbo 510(k) eSubmissions, guidance documents, and upcoming meetings and presentations about in-home and laboratory diagnostic tests.(Subscribe)
Personal Protective EquipmentInformation about personal protective equipment (PPE) regulated by FDA for use in patient care.(Subscribe)
Recent Device ApprovalsInformation about medical devices FDA has recently approved.(Subscribe)
Registration & ListingRegistration and listing provides FDA with the location of medical device establishments and the devices manufactured at those establishments.(Subscribe)
Reprocessing of Single-Use DevicesInformation about the reprocessing of single-use medical devices (SUDs).(Subscribe)
Unique Device IdentificationInformation on how the use of a Unique Device Identification (UDI) system may improve patient safety.(Subscribe)

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