28 results
·
21ms
·
Sources: EU EUDAMED, US FDA
SONICWAVE SONIC PLAQUE REMOVER
FDA 510(k)
FDA Class 1
·Dental
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0120140·Screwdriver, Polyaxial, Standard, Cannulated, L...
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304134199·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304134250·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304134212·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304134274·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304134175·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304134311·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304134137·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304134298·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304134151·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304134236·
HYDRO2, HS-75
FDA 510(k)
FDA Class 2
·Ophthalmic
BEAUTIFIL
FDA 510(k)
FDA Class 2
·Dental
UNKNOWN PLASMABLADE DEVICE
FDA Adverse Event
Malfunction
·MEDTRONIC ADVANCED ENERGY, LLC·Product code DWG·August 4, 2014
PULSAR 2 GENERATOR
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY·Product code MUL·August 4, 2014
PLASMABLADE 3.0 WIDE SPATULA
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY, LLC·Product code DWG·August 4, 2014
CUP: MPACT ACETABULAR SHELL Ø48 NO-HOLE
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·January 4, 2023
LEADER 1CC X 31G INS SYR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FMF·February 25, 2013
SECUR-FIT HA PSL CUP/CLUSTER SHELL 50MM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·March 1, 2011