Dentium Co., Ltd.

3 devices · 16 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.

• NR Line GFX3011S

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  10 reports
• NR Line GFX3009S

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  3 reports
• NR Line GFX3013S

  IMPLANT, ENDOSSEOUS, ROOT-FORM
  3 reports