89 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SIC 8000
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AGXO
FDA UDI
Oticon A/S·05707131281807·H150V2, BTE 13 WL 100 CNB AGXO
BIOMET KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304207936·
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868241611·
STRYKER SWITCHPOINT INFINITY 3 CONTROL SYSTEM, MODEL: 067-8001-000
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CLAVICULAPLATE WITH ANGULAR STABLITY BONE PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BIOMET BONE CEMENT R 40X2
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·November 9, 2016
BIOMET BONE CEMENT V
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·December 1, 2016
BIOMET BONE CEMENT V
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·December 1, 2016
OPTIPAC-S 60 REFOBACIN BONE CEMENT R
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·June 14, 2016
REFOBACIN BONE CEMENT R 2X40G
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·February 2, 2018
OPTIPAC-S KNEE REFOBACIN PLUS BONE CEMNT
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·May 25, 2016
BIOMET BONE CEMENT 1X40G
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·July 22, 2016
BIOMET BONE CEMENT R 2X40G
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·July 9, 2016
OPTIPAC-S 60 REFOBACIN BONE CEMENT R
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·May 23, 2016
OPTIPAC-S 40 REFOBACIN PLUS BONE CEMENT
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·May 25, 2016
OPTIPAC-S 40 REFOBACIN PLUS BONE CEMENT
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·May 25, 2016
BIOMET BONE CEMENT V
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·December 1, 2016
BIOMET BONE CEMENT 1X40G
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·July 20, 2016
BIOMET BONE CEMENT R 40
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·September 30, 2016