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13,623 catalysts · 3,603 8k filing · 2,401 grant · 2,100 approval · 1,445 device 510k · 1,074 device recall · 1,000 device adverse event
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13,623 catalysts · 3,603 8k filing · 2,401 grant · 2,100 approval · 1,445 device 510k · 1,074 device recall · 1,000 device adverse event
Inappropriate/Inadequate Shock/Stimulation
Premature Discharge of Battery
Fluid/Blood Leak; Mechanical Problem
Adverse Event Without Identified Device or Use Problem
Charging Problem
Adverse Event Without Identified Device or Use Problem
Failure to Seal
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Fluid/Blood Leak
Failure to Osseointegrate
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Device Handling Problem
Device Handling Problem
Device Handling Problem
Appropriate Term/Code Not Available
Device Handling Problem
Appropriate Term/Code Not Available
Adverse Event Without Identified Device or Use Problem
Device Appears to Trigger Rejection
Device Handling Problem
Appropriate Term/Code Not Available
Appropriate Term/Code Not Available
Battery Problem
Therapeutic or Diagnostic Output Failure
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Use of Incorrect Control/Treatment Settings
Improper or Incorrect Procedure or Method
Detachment of Device or Device Component
Device Appears to Trigger Rejection
Infusion or Flow Problem
Infusion or Flow Problem
Infusion or Flow Problem
Infusion or Flow Problem
Infusion or Flow Problem
Patient Device Interaction Problem
Detachment of Device or Device Component
Infusion or Flow Problem
Leak/Splash; Material Split, Cut or Torn
Adverse Event Without Identified Device or Use Problem
Premature Discharge of Battery; Pumping Stopped
Failure to Obtain Sample