16 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Invia White Foam NPWT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BI-METRIC XR-SERIES HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304650602·
MAESTRO TOTAL WRIST
FDA UDI
Biomet Orthopedics, LLC·00880304555099·
Maestro™ Total Wrist
FDA UDI
Biomet Orthopedics, LLC·00887868239939·
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486000509·MCK Patellofemoral Component
ACUPULSE 30/40 ST CO2 LASER SYSTEM AND ACUPULSE 40WG CO2 LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DEVICE MODIFICATION TO PINNACLE DESTINATION PERIPHERAL GUIDING SHEATH
FDA 510(k)
FDA Class 2
·Cardiovascular
TAPERED FINAL DRILL
FDA UDI
SWEDEN & MARTINA SPA·D7701349483·TAPERED FINAL DRILL SLEEVE 415 D.3.80 L.18.00 MM
CYLINDRICAL FINAL DRILL
FDA UDI
SWEDEN & MARTINA SPA·D7701349023·CYLINDRICAL FINAL DRILL SLEEVE 415 D.3.40 L.18....
CYLINDRICAL FINAL DRILL
FDA UDI
SWEDEN & MARTINA SPA·D7701350623·CYLINDRICAL FINAL DRILL SLEEVE 415 D.3.00 L.18....
INTERMEDIATE DRILL
FDA UDI
SWEDEN & MARTINA SPA·D7701348703·INTERMEDIATE DRILL SLEEVE 415 D.2.00 L.18.00 MM
MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·October 15, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011
SOLYX SIS SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 20, 2013
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 5/13 MM R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·April 23, 2020
BD MICROLANCE¿ HYPODERMIC NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·March 1, 2019