7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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F3D Lateral Lumbar Interbody System, CL5 Lateral Lumbar Interbody System, and Oro Lateral Plate System
FDA 510(k)
FDA Class 2
·Orthopedic
CIRONA DVT FOOT GARMENT
FDA 510(k)
FDA Class 2
·Cardiovascular
ClarifEye R1.0, ClarifEye Needle
FDA 510(k)
FDA Class 2
·Radiology
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 11, 2019
AUTOTOME RX SPHINCTEROTOME
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code KNS·September 1, 2011
*
FDA Adverse Event
Malfunction
·*·Product code KSZ·August 18, 2008
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 17, 2013