Medical Device
Safety Data
These device-safety signals come from the U.S. Food & Drug Administration (FDA) MAUDE database, which logs well over 1,000 adverse-event reports for high-volume devices, refreshed March 2026, see our methodology.
Explore 24,003,540 FDA adverse event reports across 1,000 medical devices from 443 manufacturers. Powered by the FDA MAUDE database.
Browse by Device
View adverse event data for 1,000 medical devices, including event types, patient outcomes, product problems, and yearly trends.
Browse by Manufacturer
View adverse event data for 443 medical device manufacturers, including top devices, event breakdowns, and safety trends.
Most-Reported Devices
View all →Implant, Endosseous, Root-Form
Integrated Continuous Glucose Monitoring System, Factory Calibrated
Pump, Infusion
Alternate Controller Enabled Insulin Infusion Pump
Pump, Infusion, Insulin, To Be Used With Invasive Glucose Sensor
Automated Insulin Dosing Device System, Single Hormonal Control
Pump, Infusion, Insulin
Automated Insulin Dosing , Threshold Suspend
System, Test, Blood Glucose, Over The Counter
Implantable Cardioverter Defibrillator (Non-Crt)
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
Sensor, Glucose, Invasive, Non-Adjunctive
Top Manufacturers by Reports
View all →DEXCOM, INC.
MEDTRONIC PUERTO RICO OPERATIONS CO.
CAREFUSION SD
TANDEM DIABETES CARE
INSTITUT STRAUMANN AG
NOBEL BIOCARE AB
MEDTRONIC MINIMED
BOSTON SCIENTIFIC CORPORATION
ABBOTT DIABETES CARE INC
MPRI
RESPIRONICS, INC.
INSULET CORPORATION
About This Data
The FDA Manufacturer and User Facility Device Experience (MAUDE) database contains reports of adverse events involving medical devices. Reports are submitted by manufacturers, healthcare facilities, and patients.
Important: Report counts do not indicate a device is unsafe. Higher-use devices naturally generate more reports. Events may be reported by anyone and are not verified by the FDA. Use this data as one factor alongside clinical evidence when evaluating device safety.