16 results · 25ms · Sources: EU EUDAMED, US FDA

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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