56 results · 21ms · Sources: EU EUDAMED, US FDA

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OSSE-LIGN

FDA 510(k)
FDA Class 2 ·Orthopedic

MODIFICATION TO HEARTWAVE ALTERNANS PROCESSING SYSTEM, MODEL APS

FDA 510(k)
FDA Class 2 ·Cardiovascular

HAKIM PROGRAMMER AND TRANSMITTER

FDA 510(k)
FDA Class 2 ·Neurology

PERFORMANCE TOTAL KNEE PROSTHESIS

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code HRY·October 25, 2019

PERFORMANCE DISTAL FAB LM/RL MED

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016

PERFORMANCE DISTAL FAB LL/RM MED

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

VANGRD CR POR/HA FEM - RT 72.5

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·March 31, 2016

TINBN VNGRD INT CR ANAT FEMORAL R 62.5 MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·March 31, 2016

VANGUARD CR POROUS/HA FEM - RT 72.5

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·March 23, 2016

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026

LCS COMP RP INSERT STD+ 10MM

FDA Adverse Event
Injury ·1219655 DEPUY-RAYNHAM·Product code NJL·March 27, 2013

JETSTREAM G3

FDA Adverse Event
Injury ·PATHWAY MEDICAL TECHNOLOGIES, INC.·Product code MCW·March 16, 2011