21 results · 22ms · Sources: EU EUDAMED, US FDA

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EBA One Nailing System

FDA 510(k)
FDA Class 2 ·Orthopedic

Vanguard® Knee System

FDA UDI
Biomet Orthopedics, LLC·00880304272040·

Vanguard Knee System

FDA UDI
Biomet Orthopedics, LLC·00880304466135·

XIA 3 SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

LANX LATERAL

FDA 510(k)
FDA Class 2 ·Orthopedic

FMRL PS OPEN INTL LT

FDA Adverse Event
Injury ·BIOMET INC.·Product code JWH·February 6, 2020

OCTRODE LEAD KIT, 60CM LENGTH

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code LGW·June 16, 2024

INTERSTIM II

FDA Adverse Event
Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·July 8, 2011

BEND-SCR F/UNILOCK-RECOPL TI

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code LXH·June 22, 2013

FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FRN·October 4, 2008

UNKNOWN CEMENT

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LOD·March 20, 2020

BIOMET ARCOM PATELLA

FDA Adverse Event
Death ·ZIMMER BIOMET, INC.·Product code JWH·November 8, 2018

BIOMET CC CRUCIATE TRAY

FDA Adverse Event
Death ·ZIMMER BIOMET, INC.·Product code JWH·November 7, 2018

VANGUARD PS INTERLOCKING FEMORAL

FDA Adverse Event
Death ·ZIMMER BIOMET, INC.·Product code JWH·November 8, 2018

VANGUARD TM PS OPEN BOX FEMORAL - 72.5 MM LEFT-INTERLOK

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·May 5, 2017

BIOMET FIXED I-BEAM TIBIAL PLATE INTERLOK - WITH LOCKING BAR

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·May 5, 2017

VANGUARD SERIES-A STANDARD PATELLA ARCOM THREE 1/4" PEGS

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·May 5, 2017

UNKNOWN FEMORAL COMPONENT

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 20, 2020

SERIES A ASYMMETRIC PAT 34X8.5

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 20, 2020

BIOMET CC CRUCIATE TRAY 79MM MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 20, 2020