16 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MONOBLOCK PRESS-FIT HIP STEM
FDA 510(k)
FDA Class 2
·Orthopedic
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA UDI
FX SOLUTIONS·03701037312506·HUMELOCK REVERSED RIGHT DELTO PECTORAL CUTTING ...
TMA - Archwire
FDA UDI
ORMCO CORPORATION·00889989026405·ARCH ALXLOOP TMA 17X25 M/U 38MM PK/5
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0600020·Tray Insert, Level 2
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0600120·Tray Insert 5, Cosmolock Deformity
DORNIER MEDILAS D SKINPULSE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
POWDER FREE PURPLE NITRILE EXAMINATION GLOVES, NONSTERILE
FDA 510(k)
FDA Class 1
·General Hospital
INTRALASE FS2
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HNO·November 21, 2013
BD PRECISIONGLIDE
FDA Adverse Event
Injury
·BD·Product code FMI·November 22, 2013
VISX EXCIMER LASER
FDA Adverse Event
Injury
·AMO MANUFACTURING USA LLC·Product code LZS·November 5, 2010
INTRALASE FS2
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HNO·August 20, 2013
INTRALASE FS2
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HNO·October 30, 2013
EON MINI
FDA Adverse Event
Death
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 11, 2013
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·June 12, 2008
3500
FDA Adverse Event
Malfunction
·SMITHS MEDICAL·Product code FRN·April 5, 2011
BD PRECISIONGLIDE¿ NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·November 21, 2018