9 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACUFEX FIXATION POST
FDA 510(k)
FDA Class 2
·Orthopedic
APEX Revision Knee
FDA UDI
Omni Life Science, Inc.·00841690114277·PS-R Insert, Size 5 x 14mm
Solstice Occipito-Cervico-Thoracic System
FDA UDI
Life Spine, Inc.·00190837017125·
Duo Lumbar Interbody Fusion Device
FDA UDI
SPINEOLOGY INC.·M7402924514·Duo, Hyper-Lordotic, 45 x 14mm
STRUNG TELFA NON-ADHERENT SPONGE
FDA 510(k)
FDA Class 2
·Neurology
1.9 FRENCH LITHOTRIPTER ELECTRODE, MODIFICATION
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LYNX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·January 22, 2013
ENRHYTHM DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code DXY·December 14, 2010
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 9, 2014