28 results · 23ms · Sources: EU EUDAMED, US FDA

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Suprasorb A + Ag “R”

FDA 510(k)
FDA Unclassified ·Unknown

Vanguard® Knee System

FDA UDI
Biomet Orthopedics, LLC·00880304438866·

FX V 135 stem

FDA UDI
FX SOLUTIONS·03701037315125·FX V 135 stem TA6V Ø32/08 cementless Ti/HA

REVERSE SHOULDER PROSTHESIS MONOBLOCK STEM

FDA 510(k)
FDA Class 2 ·Orthopedic

SATURN ACTIVE LASER SYSTEM

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

VANGUARD SERIES-A STANDARD PATELLA

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 9, 2018

VNGD PS TIB BRG 12X71/75MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

COLLEAGUE CX VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 3, 2008

ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

FDA Adverse Event
Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·June 21, 2013

FLEXCATH STEERABLE SHEATH

FDA Adverse Event
Malfunction ·MEDTRONIC CRYOCATH LP·Product code DRA·July 28, 2011

BIOMET ARCOM 3 PEG/POST

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

VNGD PS TIB BRG 12X71/75MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

BIOMET CC I-BEAM TRAY 75MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

BIOMET FIXED CRUCIATE TIBIAL PLATE INTERLOK - WITH LOCKING BAR

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 10, 2018

VANGUARD PS+ TIBIAL BEARING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 10, 2018

TRUE METRIX AIR

FDA Adverse Event
Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·October 12, 2021

DENALI JUGULAR SYSTEM

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 27, 2023

VANGUARD DCM PS TIBIAL BEARING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·November 5, 2017

DENALI JUGULAR SYSTEM

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·November 21, 2023

DENALI FEMORAL SYSTEM

FDA Adverse Event
Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 10, 2023