32 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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GLUCOSE REAGENT FOR BECKMAN SYNCHRON CX & CX DELTA SYSTEMS
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Baltic Denture System BD Load
FDA UDI
Merz Dental GmbH·D7091033055·Baltic Denture System BDLoad ↓ Ln6 PLSEum4DFl D...
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0330150·Coronal Bender, Left
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0330050·Vise Grip, Large, 5.5mm
THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Dental
MEDLINE STERILE POWDER FREE LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)
FDA 510(k)
FDA Class 1
·General Hospital
BI-METRIC LAT PC 13X145MM T1
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWZ·November 9, 2016
BI-METRIC LAT PC 12X140MM T1
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·November 9, 2016
BI-METRIC LAT PC 11X135MM T1
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·November 9, 2016
BI-METRIC LAT PC 10X130MM T1
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·November 9, 2016
BI-METRIC LAT PC 9X125MM T1
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWZ·November 9, 2016
SPIDERCUP
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·January 3, 2019
SPIDERCUP
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code PBI·January 3, 2019
UNKNOWN STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·November 9, 2018
RINGLOC MODULAR ACETABULAR SYSTEM
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code LPH·March 29, 2023
14X150MM BI-METRIC FEMORAL COLLARLESS STEM WITH TYPE 1 TAPER
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·September 23, 2016
BI-METRIC FEMORAL COMPONENTS
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·March 15, 2017
2800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 1, 2013
TRUFILL DCS ORBIT DETACHABLE COILS COMPLEX
FDA Adverse Event
Malfunction
·CORDIS NEUROVASCULAR, INC.·Product code HCG·March 30, 2011
LIFEPAK CR PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·April 23, 2008