Bicon, LLC

7 devices · 9 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.

• Integra-CP 260-340-258

  Implant, Endosseous, Root-Form
  2 reports
• Integra-CP 260-350-306

  Implant, Endosseous, Root-Form
  2 reports
• Integra-Ti 260-145-306

  Implant, Endosseous, Root-Form
  1 report
• Integra-CP 260-340-251

  Implant, Endosseous, Root-Form
  1 report
• Integra-CP 260-340-256

  Implant, Endosseous, Root-Form
  1 report
• Integra-CP 260-345-258

  Implant, Endosseous, Root-Form
  1 report
• Integra-CP 260-360-305

  Implant, Endosseous, Root-Form
  1 report