7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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THE OMNIFIT EPF HIP JOINT FEMORAL STEM
FDA 510(k)
FDA Class 2
·Orthopedic
MEDILOG 9000-II AMBULATORY RECORDER
FDA 510(k)
FDA Class 2
·Cardiovascular
VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
OLYMPUS THUNDERBEAT 5 MM, 35 CM, FRONT ACUATED
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEM CORPORATION·Product code GEI·May 20, 2014
TOTALCARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·November 20, 2012
DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·November 10, 2010
Exactech Equinoxe REVERSE SHOULDER,42mm Constrained Humeral Liner, a) +0mm, Item number 320-42-10, b) +2.5mm, Item Number 320-42-13; Shoulder Arthroplasty
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·April 10, 2024