16 results
·
25ms
·
Sources: EU EUDAMED, US FDA
INTROL BLADDER NECK SUPPORT PROSTHESIS WITH REMOVAL TOOL
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809665583307·MIS Cannulated Screw, Ø5.0 x 40mm, Ø6.0mm Rod
Eye Shield
FDA UDI
KATENA PRODUCTS, INC.·00841668111161·FOX EYE SHIELD GARTERS WHITE PACK OF 50
Restore
FDA UDI
KEYSTONE DENTAL, INC.·D768R96504004K0·Healing Abutment
Restore
FDA UDI
KEYSTONE DENTAL, INC.·D768R96504003K0·Healing Abutment
Restore
FDA UDI
KEYSTONE DENTAL, INC.·D768R96504006K0·Healing Abutment
Restore
FDA UDI
KEYSTONE DENTAL, INC.·D768R96504002K0·Healing Abutment
TELEPULSE
FDA 510(k)
FDA Class 2
·Anesthesiology
ALGINATE FIBER
FDA 510(k)
FDA Unclassified
·Unknown
UNICEL DXC 800 SYNCHRON SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JGS·February 21, 2012
XMAX MOTOR
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code ERL·March 31, 2015
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 15, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011
ENTOVIS DR-T PROMRI
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code DXY·July 29, 2014
2.7 Degree Straight Sagittal Saw attachment (Mako Total Knee Application and Partial Knee Application 3.0)
FDA Recall
Terminated
·Mako Surgical Corporation·Product code OLO·April 25, 2019
2.7 Degree Angled Sagittal Saw attachment (Mako Total Knee Application Only)
FDA Recall
Terminated
·Mako Surgical Corporation·Product code OLO·April 25, 2019