26 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CHRONOS TRICALCIUM PROSPHATE (CHRONOS TCP)
FDA 510(k)
FDA Class 2
·Orthopedic
Diamond D
FDA UDI
Keystone Industries·H66810130721·Denture Acrylic HC 25 lb Chroma Essence P&L
16PW - Piedmont Natural Gas - Poly White
FDA UDI
Certified Safety Manufacturing, Inc.·00766588130729·16PW - Piedmont Natural Gas - Poly White
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0130120·Segmental Rod Reducer Driver
InTess C Cervical Cage System
FDA UDI
Kalitec Direct LLC·B07309K01307N0·Cervical Rasp, 14 x 11, 7mm, 0 Degree, No Taper
POWDER FREE PURPLE NITRILE EXAMINATION GLOVES, NONSTERILE
FDA 510(k)
FDA Class 1
·General Hospital
PACING LEADS, GUIDE WIRES, AND VARIOUS ACCESSORIES
FDA 510(k)
FDA Class 3
·Cardiovascular
SYNCHRON VANCOMYCIN REAGENT
FDA Adverse Event
BECKMAN COULTER INC.·Product code LEH·June 10, 2011
SCHILLER
FDA Adverse Event
Malfunction
·SCHILLER AG·Product code MHX·November 2, 2006
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017
DISC LT DSTL HMRL BDY SET
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDC·April 1, 2019
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 19, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 19, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code JDC·May 19, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 19, 2017
MED-EL COMBI 40+ COCHLEAR IMPLANT SSYTEM
FDA Adverse Event
Malfunction
·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·March 15, 2013
SPRINT FIDELIS
FDA Adverse Event
Death
·MEDTRONIC, INC.·Product code LWS·March 10, 2011
SLIMLINE EZ 200
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code GEX·March 5, 2008