Biotechnology Institute Sl

107 devices · 375 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.

• INTERNA IMPLANT, NARROW PLATFORM, CORE-X® CA D:4.25 L:8.5 IIPEXCA4285

  Implant, Endosseous, Root-Form
  1 report
• INTERNA IMPLANT, NARROW PLATFORM, CORE-X® CA D:4.75 L:6.5 IIPEXCA4765

  Implant, Endosseous, Root-Form
  1 report
• INTERNA IMPLANT, NARROW PLATFORM, CORE-X® CA D:4.75 L:8.5 IIPEXCA4785

  Implant, Endosseous, Root-Form
  1 report
• INTERNA IMPLANT, NARROW PLATFORM, CORE-X® CA D:4.25 L:13 IIPEXCA4213

  Implant, Endosseous, Root-Form
  1 report
• INTERNA IMPLANT, NARROW PLATFORM, CORE-X® CA D:4.5 L:10 IIPEXCA4510

  Implant, Endosseous, Root-Form
  1 report
• INTERNA IMPLANT, NARROW PLATFORM, CORE-X® CA D:3.75 L:11.5 IIPEXCA3711

  Implant, Endosseous, Root-Form
  1 report
• INTERNA IMPLANT, NARROW PLATFORM, CORE-X® CA D:3.75 L:7.5 IIPEXCA3775

  Implant, Endosseous, Root-Form
  1 report