Catalyst Orthoscience Inc.

9 devices · 21 adverse event reports · 0 devices named in recalls

Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.

All Catalyst Orthoscience Inc. devices

• R1 Reverse Shoulder System 1230-7504-002

  Shoulder Prosthesis, Reverse Configuration
  5 reports
• R1 Reverse Shoulder System 1230-7505-003

  Shoulder Prosthesis, Reverse Configuration
  4 reports
• R1 Reverse Shoulder System 1230-7504-004

  Shoulder Prosthesis, Reverse Configuration
  3 reports
• R1 Reverse Shoulder System 1230-7505-002

  Shoulder Prosthesis, Reverse Configuration
  3 reports
• R1 Reverse Shoulder System 1230-7504-003

  Shoulder Prosthesis, Reverse Configuration
  2 reports
• R1 Reverse Shoulder System 1230-7505-004

  Shoulder Prosthesis, Reverse Configuration
  1 report
• R1 Reverse Shoulder System 1230-7512-002

  Shoulder Prosthesis, Reverse Configuration
  1 report
• R1 Reverse Shoulder System 1230-7513-002

  Shoulder Prosthesis, Reverse Configuration
  1 report
• EA Convertible System 1231-7602-001

  Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
  1 report