236 results · 68ms · Sources: EU EUDAMED, US FDA

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BIOMET ORTHOPEDICS INC

FDA Adverse Event
Malfunction ·BIOMET ORTHOPEDICS, INC·Product code HTY·September 18, 2003

BIOMET ORTHOPEDICS, INC.

FDA Adverse Event
Injury ·BIOMET, INC.·Product code JDI·June 23, 2005

BIOMET ORTHOPEDICS, INC.

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·January 12, 2007

BIOMET ORTHOPEDICS INC

FDA Adverse Event
Injury ·BIOMET, INC.·Product code JDI·January 18, 2008

BIOMET ORTHOPEDICS, INC.

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS, INC.·Product code JWH·January 7, 2008

BIOMET ORTHOPEDICS, INC

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS, INC·Product code HSA·December 12, 2002

BIOMET ORTHOPEDICS, INC

FDA Adverse Event
Injury ·BIOMET ORTHPEDICS, INC·Product code HWC·October 15, 2002

BIOMET ORTHOPEDICS, INC. REPICCI II

FDA Adverse Event
Malfunction ·BIOMET ORTHOPEDICS, INC.·Product code JWH·January 31, 2005

E-POLY 40MM RINGLOC ACETABULAR LINER +3 HI-WALL SIZE 24

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code MAY·December 3, 2010

ST GOBAIN

FDA Adverse Event
Other ·CERAMIQUES AVANCEES DESMARQUES·Product code JDI·January 13, 2003

BIOMET ORTHOPEDIC, INC

FDA Adverse Event
Injury ·BIOMET ORTHOPEDIC, INC·Product code JDI·February 22, 2008

VANGUARD CR TIBIA BEARING 10X63/67

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·November 27, 2012

M2A MAGNUM MODULAR HEAD 50MM HEAD DIAMETER

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 28, 2010

22.2MM DIA COCR MODULAR HEAD -5 NK

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·September 24, 2013

BIOMET ORTHOPEDICS M2A MAGNUM

FDA Adverse Event
Injury ·BIOMET INC.·Product code KWA·November 9, 2021

ACE LONG TROCANTERIC NAIL RIGHT, 130, 380 MM, 9 DIA

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC·Product code HSB·September 19, 2014

TAPERLOC FEMORAL STEM

FDA Adverse Event
Injury ·BIOMET UK LTD·Product code LPH·December 2, 2010

LONGEVITY CONST LINER 50X28

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWZ·September 16, 2025

BONE SCREW SELF-TAPPING 6.5 MM DIA. 20 MM LENGTH

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 15, 2025

BONE SCREW SELF-TAPPING 6.5 MM DIA. 25 MM LENGTH

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 15, 2025