27 results
·
20ms
·
Sources: EU EUDAMED, US FDA
KINETIC CANNULA
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040008355·Zirlux 16+ A2 89x17x16
Ocata Anterior Cervical System
FDA UDI
Kalitec Direct LLC·B07308K0120020·Driver Shaft, Final Tighten
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0100420·Assembly, Caddie, Adjustable Cross Links
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0120020·T-Handle, T25, Screw Height Adjuster
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0120120·Screwdriver, NIDO Assembled Screws, Sleeved
TRUCONE ROTATIONAL CONE BIOPSY INSTRUMENT, MODEL 231812 - 233018
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CT PERFUSION 2
FDA 510(k)
FDA Class 2
·Radiology
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
2520274-2013-01599
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·March 20, 2013
BRAVO
FDA Adverse Event
Malfunction
·GIVEN IMAGING LTD.·Product code FFT·February 28, 2011
ORTHO SUMMIT SAMPLE HANDLING SYSTEM
FDA Adverse Event
Malfunction
·HAMILTON BONADUZ AG·Product code JTC·February 8, 2008
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017