15 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Sonoma Cancellous Bone Screw and Washer
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04064984699588·GENUMEDI PSS BLUE, SIZE VI
OSS™ Orthopedic Salvage System
FDA UDI
Biomet Orthopedics, LLC·00880304239043·
Oticon
FDA UDI
Oticon A/S·05707131287663·H10V2, RITE 312 WL STG
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962104361·ROUND BURR, 4.5MM, COMPATIBLE W/SN
PROWIN
FDA 510(k)
FDA Class 2
·Radiology
EVERON CENTRAL DISPLAY STATION - CDS, MODEL VERSION 1.0.0
FDA 510(k)
FDA Class 2
·Cardiovascular
HNM MEDICAL
FDA UDI
HNM STAINLESS, LLC.·00842962102374·DISPOSABLE ARTHROSCOPIC 4.5mm ROUND BURR, COMPA...
ADVANCE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·May 31, 2013
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·June 7, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 7, 2014
COBALT HV W/ GENTAMICIN POWDER BONE CEMENT 40 GRAMS
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LOD·October 2, 2017
COBALT HV W/ GENTAMICIN POWDER BONE CEMENT 40 GRAMS
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LOD·October 6, 2017
ONCOLOGY SALVAGE SYSTEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·March 10, 2017
ORTHOPEDIC SALVAGE SYSTEM DIAPHYSEAL SEGMENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·February 21, 2018