Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Medsun Reports
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

We regret to inform you that the Medical Product Safety Network (MedSun) search option is currently unavailable. While data prior to July 2024 is still accessible, the database is not being updated at this time. Our team is working diligently to resolve this issue. Thank you for your patience and understanding.

Please note that medical device reports that have been received through the MedSun program are included in the Manufacturer and User Facility Device Experience (MAUDE) Database, which continues to be regularly updated.

The Medical Product Safety Network (MedSun) is an adverse event reporting program launched in 2002 by the U.S. Food and Drug Administration’s Center for Devices and Radiological Health (CDRH). The primary goal for MedSun is to work collaboratively with the clinical community to identify, understand, and solve problems with the use of medical devices.

Learn more...

Search Database Help






use calendar to select date 		  to  
use calendar to select date
February 20, 2002 is the earliest date for searching medsun reports.
 
Other Databases
-
-