8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
ELVI 840 AGGREGOMETER
FDA 510(k)
FDA Class 2
·Hematology
EXTREMITY MEDICAL MIDFOOT SCREW SYSTEM, CHARCX, INTRAMEDULLARY SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Willow Wearable Breast Pump 2.0
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
NV GXL LINR, NTRL, 36MM ID, GROUP 4 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·August 26, 2024
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 6, 2014
REVEAL DX
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code DSI·October 15, 2012
VIRTUOSO VR
FDA Adverse Event
MEDTRONIC S.A.·Product code LWS·August 10, 2010
Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089; CD1235-40/100029272, 100029282, 100029311, 100031039, 100059779; CD1235-40Q/100029273, 100029295, 100029312, 100030840; CD1241-40/100046351; CD1241-40Q/100046167; CD2231-40/100029274, 100030110, 100041922; CD2231-40Q/100029275, 100030089, 100041923; CD2233-40/100029147, 100029276, 100029313, 100031066, 100037043, 100048759, 100070007; CD2233-40Q/100029148, 100029263, 100029314, 100031067, 100037044, 100059770, 100070068; CD2235-40/100029149, 100029265, 100029283, 100031029, 100059837; CD2235-40Q/100029239, 100029258, 100029284, 100031030, 100066504; CD2241-40/100046148; CD2241-40Q/100046149; CD2299-40/100056952
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018