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14,970 catalysts · 3,605 8k filing · 2,670 grant · 2,420 approval · 1,702 device 510k · 1,263 device recall · 1,164 device pma
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14,970 catalysts · 3,605 8k filing · 2,670 grant · 2,420 approval · 1,702 device 510k · 1,263 device recall · 1,164 device pma
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
Difficult to Remove; Material Twisted/Bent
Mechanical Jam; Activation Problem
Adverse Event Without Identified Device or Use Problem
Device Dislodged or Dislocated
Insufficient Information