30 results · 32ms · Sources: EU EUDAMED, 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