7 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PATIENT SPECIFIC ACETABULAR RECONSTRUCTION PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
PRECLUDE PERICARDIAL MEMBRANE
FDA 510(k)
FDA Class 2
·Cardiovascular
SALUMEDICA NERVE CUFF
FDA 510(k)
FDA Class 2
·Neurology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 18, 2025
AS3000
FDA Adverse Event
MINDRAY DDS USA, INC.·Product code BSZ·April 30, 2013
CHARGING SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·September 3, 2014
SCREW-IN
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·May 18, 2011