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

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Praxiject 0.9% NaCl

FDA 510(k)
FDA Class 2 ·General Hospital

ECHO BI-METRIC HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304463370·

Echo® Bi-Metric® Hip System

FDA UDI
Biomet Orthopedics, LLC·00887868260759·

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690198697·AK3 Ultra Insert Trial Size 4, 14mm

OsteoMed

FDA UDI
OSTEOMED LLC·00845694009690·2.4mm x 14mm Cannulated Lag Screw

Responsive Orthopedics Total Knee Arthroplasty System

FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973108115·TRIAL 90-SRK-192414 POLY-MPCS 4X14 LEFT

OsteoMed

FDA UDI
OSTEOMED LLC·00845694070669·Cannulated 2.4 x 14mm Lag Screw Sterile Qty 5

CONMED DETACHATIP INSTRUMENT TRAY, 33CM AND 43CM

FDA 510(k)
FDA Class 2 ·General Hospital

ELIA B2-GLYCOPROTEIN I IGA IMMUNOASSAY

FDA 510(k)
FDA Class 2 ·Immunology

POUNCE VENOUS THROMBECTOMY SYSTEM

FDA Adverse Event
Injury ·SURMODICS INC·Product code QEW·May 16, 2024

CER BIOLOXD OPTION HD 40MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LZO·October 26, 2017

NXSTAGE SYSTEM ONE

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·October 7, 2008

GDC VORTX 2MM X 5MM

FDA Adverse Event
Injury ·STRYKER NEUROVASCULAR CORK·Product code HCG·June 27, 2013

FLOGARD

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 5, 2011

ECHO BI-METRIC HIP SYSTEM STANDARD FEMORAL STEM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·June 28, 2018

BIOLOX DELTA CERAMIC FEM HD 36/+3MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LZO·December 15, 2025

G7 VIT E 10DEG LNR 36MM G

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·August 15, 2022

M2A-MAGNUM MOD HD SZ 44MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWY·January 2, 2019

M2A-MAGNUM PF CUP 50ODX44ID

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·January 2, 2019

ECHO Bi-Metric Hip System, Reduced Proximal Profile, Standard 135o neck, item number 192414. orthopedic hip prosthesis femoral stem

FDA Recall
Terminated ·Zimmer Biomet, Inc.·Product code KWA·June 8, 2018