9 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Stryker Integrated Bipolar Cord and Tubing Sets
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LINEAR? ST
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 1, 2026
OPTIGEN TOTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
REPIPHYSIS LIMB SALVAGE PROXIMAL FEMUR AND TOTAL FEMUR
FDA 510(k)
FDA Class 2
·Orthopedic
8041187-2017-00082
FDA Adverse Event
Malfunction
·August 24, 2017
GMK-HINGE FEMORAL COMPONENT SIZE 3 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KRO·July 25, 2022
TERUMO ADVANCED PERFUSION SYSTEM 1
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·October 9, 2014
ARTICULEZE M HEAD 36MM +12
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 17, 2013
ACCU-CHEK SPIRIT
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·June 17, 2011