25 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
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