5 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
K140347
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·May 6, 2021
K140347
FDA Adverse Event
Injury
·DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)·Product code DZE·May 6, 2021
ENERGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 3, 2014
HT POWERTURN
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code DQX·May 31, 2013
GEM PREMIER 4000
FDA Adverse Event
Malfunction
·INSTRUMENTATION LABORATORY CO.·Product code MZV·June 17, 2011