81 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IPS CaseDesigner
FDA 510(k)
FDA Class 2
·Radiology
COTTLE-DORSAL SCISSORS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896055780·COTTLE-DORSAL SCISSORS HEAVY SERRATED BLADES PO...
Zavation
FDA UDI
Zavation LLC·00842166131903·Ti3Z CIF 12mmx14mmx10mm -8 deg
OsteoMed
FDA UDI
OSTEOMED LLC·00845694060813·1.6mm Plating Module, ICON
Arena-C®
FDA UDI
SPINEFRONTIER, INC.·00190361021124·12x15 Arena-C HA PEEK Lordotic 10mm
QUALITROL LIPID CONTROL, LEVELS 1 AND 2
FDA 510(k)
FDA Class 1
·Clinical Chemistry
VIDAS D-DIMER NEW (DD2) ASSAY MODEL#30 442
FDA 510(k)
FDA Class 2
·Hematology
ULTRACINCH
FDA Adverse Event
Malfunction
·EPICOR MEDICAL INC.·Product code LPB·April 9, 2008
Widex
FDA UDI
Widex A/S·05706069726244·Widex mind220 M2-X ITE (Clay brown S-220 ) Tele...
Widex
FDA UDI
Widex A/S·05706069724851·Widex D-CIC (Clay brown S-220 ) Left, RC coil
Widex
FDA UDI
Widex A/S·05706069725216·Widex EVOKE E-IP (Clay brown S-220 ) Right
Widex
FDA UDI
Widex A/S·05706069725810·Widex EVOKE E-CIC (Clay brown S-220 ) Left, RC ...
Widex
FDA UDI
Widex A/S·05706069724493·Widex UNIQUE U-CIC L (Clay brown S-220 ) Left, ...
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·November 7, 2008
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·November 7, 2008
1043534-2012-01251
FDA Adverse Event
Malfunction
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JWH·October 2, 2012
LIGASURE STD DISP ELECT/CORD
FDA Adverse Event
Injury
·COVIDIEN LLP·Product code GEI·September 20, 2013
LIGASURE STD DISP ELECT/CORD
FDA Adverse Event
Injury
·COVIDIEN LP·Product code GEI·September 20, 2013
MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·September 2, 2008
LIGASURE STD DISP ELECT/CORD
FDA Adverse Event
Injury
·COVIDIEN LP·Product code GEI·September 20, 2013