14 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OsseoFit Stemless Shoulder System
FDA 510(k)
FDA Class 2
·Orthopedic
RANGE/MESA/DENALI SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
AEQUALIS REVERSED SHOULDER PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
TORNIER AEQUALIS REVERSE SHOLDER PROSTHESIS
FDA Adverse Event
Malfunction
·TORNIER INC.·Product code HSD·June 18, 2009
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 29, 2025
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0CM NON US
FDA Adverse Event
Malfunction
·COSTA RICA·Product code LTI·November 18, 2008
EVERCROSS¿ PTA BALLOON
FDA Adverse Event
Injury
·EV3 INC.·Product code DQY·September 9, 2011
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·July 22, 2013
BIOMET MICROFIXATION STERNALOCK BLU STERNAL CLOSURE SYSTEM
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HRS·May 21, 2015
BIOMET MICROFIXATION STERNALOCK BLU STERNAL CLOSURE SYSTEM
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HRS·May 21, 2015
BIOMET MICROFIXATION STERNALOCK BLU STERNAL CLOSURE SYSTEM
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HRS·May 21, 2015
BIOMET MICROFIXATION STERNALOCK BLU STERNAL CLOSURE SYSTEM
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HRS·May 21, 2015
BIOMET MICROFIXATION STERNALOCK BLU STERNAL CLOSURE SYSTEM
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HRS·May 21, 2015
BIOMET MICROFIXATION STERNALOCK BLU STERNAL CLOSURE SYSTEM
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HRS·May 21, 2015