19 results · 31ms · Sources: EU EUDAMED, US FDA

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Mammomat Revelation

FDA 510(k)
FDA Class 2 ·Radiology

GE LOGIQ BT08 DIAGNOSTIC ULTRASOUND SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

POSTERIOR LATERAL PLATES

FDA 510(k)
FDA Class 2 ·Orthopedic

OPTIPAC 60 REFOB BONE CMT R-3

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·May 11, 2026

PHYSIOMESH OVAL

FDA Adverse Event
Injury ·ETHICON INC.·Product code FTL·October 15, 2014

ECHELON*FLEX60 ARTICULATING

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 23, 2011

MARYLAND BIPOLAR FORCEPS INSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 17, 2013

NEOCIS GUIDANCE SYSTEM

FDA Adverse Event
Injury ·NEOCIS INC.·Product code PLV·September 13, 2019

BIOMET BONE CMENT R 1X40 JP

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·May 22, 2025

REFOBACIN BONE CEMENT R 1X40-3

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·June 18, 2025

OPTIPAC 80 BIOMET BC R

FDA Adverse Event
Death ·BIOMET FRANCE S.A.R.L.·Product code LOD·April 9, 2026

BIOMET BONE CEMENT R 40 -3

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·July 31, 2025

BIOMET BONE CMENT R 1X40 JP

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·June 17, 2025

OPTIPAC 60 REFOB BONE CMT R-3

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·February 5, 2025

OPTIPAC 60 REFOB BONE CMT R-3

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·February 5, 2025

BIOMET BONE CMENT R 1X40 JP

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·October 8, 2025

BIOMET BONE CMENT R 1X40 JP

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·October 8, 2025

BIOMET BONE CMENT R 1X40 JP

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LOD·April 8, 2025

OPTIPAC 80 BIOMET BC R

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·February 21, 2025