Densitometer, bone

FDA product code KGI · Class 2 · 7 devices · 11 reports · 5 devices named in recalls

• Horizon A

  Hologic, Inc. · Densitometer, bone
  1 recall3 reports
• Horizon Ci

  Hologic, Inc. · Densitometer, bone
  1 recall1 report
• Horizon W

  Hologic, Inc. · Densitometer, bone
  1 recall1 report
• Horizon C

  Hologic, Inc. · Densitometer, bone
  1 recall0 reports
• Horizon Wi

  Hologic, Inc. · Densitometer, bone
  1 recall0 reports
• Discovery Wi

  Hologic, Inc. · Densitometer, bone
  5 reports
• Prodigy F2

  GE Medical Systems, Ultrasound & Primary Care Diagnostics LLC · Densitometer, bone
  1 report