26 results · 24ms · Sources: EU EUDAMED, 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