30 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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WishBone Medical Plate and Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
Mako
FDA UDI
MAKO SURGICAL CORP.·00848486016593·Tibial Bearing Insert
Mako
FDA UDI
MAKO SURGICAL CORP.·00848486016630·Tibial Bearing Insert
Mako
FDA UDI
MAKO SURGICAL CORP.·00848486016616·Tibial Bearing Insert
Mako
FDA UDI
MAKO SURGICAL CORP.·00848486016609·Tibial Bearing Insert
Mako
FDA UDI
MAKO SURGICAL CORP.·07613327386172·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 6 - 9 MM
Mako
FDA UDI
MAKO SURGICAL CORP.·07613327386134·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 6 - 12 MM
Mako
FDA UDI
MAKO SURGICAL CORP.·07613327386080·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 6 - 10 MM
Mako
FDA UDI
MAKO SURGICAL CORP.·07613327386127·MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 6 - 8 MM
KIRSCHNER AND GUIDE WIRES
FDA 510(k)
FDA Class 2
·Orthopedic
ACTIFUSE SHAPE BONE GRAFT SUBSTITUTE
FDA 510(k)
FDA Class 2
·Orthopedic
GM HELIX IMPLANT 6.0X10
FDA Adverse Event
Injury
·NEODENT - JJGC S.A.·Product code DZE·March 2, 2019
INRATIO PT/INR TEST STRIPS
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·August 4, 2016
DUO-VENT CLEARLINK LUER ACTIVATED VALVE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·September 29, 2022
CLEARLINK LUER ACTIVATED VALVE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·October 31, 2022
CLEARLINK LUER ACTIVATED VALVE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·November 1, 2022
GM HELIX IMPLANT 6.0X8 MM
FDA Adverse Event
Injury
·NEODENT - JJGC S.A.·Product code DZE·March 21, 2019
NI
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·May 5, 2023
GM HELIX IMPLANT 6.0X10
FDA Adverse Event
Injury
·NEODENT - JJGC S.A.·Product code DZE·March 20, 2019
INRATIO2 PT/INR TEST STRIP
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·March 30, 2016