MEDENTiKA GmbH
2 devices · 12 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.
- MEDENTiKA 5-01-09IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- MEDENTiKA 5-01-08IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports