calendar
1,284 catalysts · 18,987 approval · 5,000 device 510k · 4,728 grant · 3,827 phase readout · 2,121 8k filing · 2,000 device pma
next 91 dayslessmore
MonWedFri
1,284 catalysts · 18,987 approval · 5,000 device 510k · 4,728 grant · 3,827 phase readout · 2,121 8k filing · 2,000 device pma
no tagged catalysts yet
Anticipated earnings call for CSL LTD ($CSLLY).
Anticipated earnings call for Beyond Air, Inc. ($XAIR).
Anticipated earnings call for Haleon plc ($HLN).
Anticipated earnings call for SMITH & NEPHEW PLC ($SNN).
Anticipated earnings call for Scilex Holding Co ($SCLX).
Anticipated earnings call for BioXcel Therapeutics, Inc. ($BTAI).
Insufficient Information
Anticipated earnings call for Grifols SA ($GRFS).
Appropriate Term/Code Not Available
Failure to Osseointegrate
Leak/Splash; Loose or Intermittent Connection
Patient-Device Incompatibility
Malposition of Device
Insufficient Information
Failure to Osseointegrate
Insufficient Information
Loss of Osseointegration
Insufficient Information
Failure to Osseointegrate; Migration
Failure to Osseointegrate
Collapse; Fluid/Blood Leak
Insufficient Information
Incorrect, Inadequate or Imprecise Result or Readings
Patient Device Interaction Problem
Low Readings
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem
Failure to Osseointegrate
Patient Device Interaction Problem
Patient Device Interaction Problem
Adverse Event Without Identified Device or Use Problem
High Readings
Adverse Event Without Identified Device or Use Problem
Charging Problem
Material Rupture
Low Readings
Osseointegration Problem
Loss of Osseointegration
Material Rupture
Adverse Event Without Identified Device or Use Problem
Migration
Adverse Event Without Identified Device or Use Problem
Improper or Incorrect Procedure or Method
Device Appears to Trigger Rejection
Positioning Failure; Insufficient Information
Loss of Osseointegration
Insufficient Information
Adverse Event Without Identified Device or Use Problem
Adverse Event Without Identified Device or Use Problem