13 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Delight, Delight ortho, B&Lite S
FDA 510(k)
FDA Class 2
·Dental
LEONE SPA
FDA UDI
LEONE SPA·08033707018919·CALIBRA 1ST MOLAR BANDS n.LL 29
AFF (MARK I) VOLUMETRIC INFUSION PUMP
FDA 510(k)
FDA Class 2
·General Hospital
ENDOFLIP GASTRIC TUBE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
LINEAR? ST
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 22, 2026
REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER 36/+3MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·November 6, 2020
PARIETEX UGYTEX PP POSTERIOR KIT X1
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code OTP·June 12, 2013
DIMENSION® CLINICAL CHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC·Product code MMI·July 21, 2011
ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY
FDA Adverse Event
Malfunction
·COOK, INC.·Product code MIH·September 11, 2008
SHOULDER SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code HSD·April 14, 2026
REVERSE SHOULDER SYSTEM GLENOSPHERE 42X27
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·March 23, 2018
SHOULDER SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code PHX·January 23, 2026
DELTAVEN 22G 25MM
FDA Adverse Event
Malfunction
·DELTA MED SPA·Product code FOZ·October 14, 2019