12 results
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19ms
·
Sources: EU EUDAMED, US FDA
TROCAR DISPOSABLE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NO-PROFILE
FDA UDI
Biomet Sports Medicine, LLC·00880304406100·
Stern Snap Abutment Base 4.0mm (AY)
FDA UDI
STERNGOLD DENTAL LLC·00841549112706·Intended for use with dental implants to suppor...
P.F.C. HIP SYSTEM NON-POROUS FEMORAL COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 5, 2024
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 5, 2024
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 5, 2024
PROMUS ELEMENT ¿
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·January 9, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-REDWOOD CITY·Product code MGB·November 22, 2010
UNKNOWN KNEE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·July 1, 2014
TI LOW PROF NEURO CONTOUR MESH 200MM X 200MM/0.6MM RIGID
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code JEY·August 15, 2018