35 results · 29ms · Sources: EU EUDAMED, US FDA

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OSTEOMARK NTX POC

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

MILENIA (TM) FERRITIN

FDA 510(k)
FDA Class 2 ·Immunology

ULTRASONIC TABLETOP DOPPLER, MODELS SD5 AND SD6

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Malfunction ·CORDIS DE MEXICO·Product code DTK·August 11, 2011

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code DTK·August 12, 2011

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code DTK·August 11, 2011

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code DTK·August 11, 2011

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code DTK·August 11, 2011

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Malfunction ·CORDIS DE MEXICO·Product code DTK·August 11, 2011

CELL DYN SAPPHIRE ANALYZER

FDA Adverse Event
Other ·ABBOTT LABORATORIES·Product code GKZ·January 3, 2006

VISIAN ICL (IMPLANTABLE COLLAMER LENS)

FDA Adverse Event
Injury ·STAAR SURGICAL COMPANY·Product code MTA·March 7, 2013

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code MDS·February 7, 2011

CAPSUREFIX NOVUS

FDA Adverse Event
Injury ·MPRI·Product code DTB·August 8, 2014

PROSTHESIS INTERVERTEBRAL DISC

FDA Adverse Event
Injury ·SYNTHES BRANDYWINE·Product code MJO·May 18, 2015

PROSTHESIS INTERVERTEBRAL DISC

FDA Adverse Event
Injury ·SYNTHES BRANDYWINE·Product code MJO·May 18, 2015

PROSTHESIS INTERVERTEBRAL DISC

FDA Adverse Event
Injury ·SYNTHES BRANDYWINE·Product code MJO·May 18, 2015

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Malfunction ·CORDIS DE MEXICO·Product code DTK·August 11, 2011

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Malfunction ·CORDIS DE MEXICO·Product code DTK·August 11, 2011

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Malfunction ·CORDIS DE MEXICO·Product code DTK·August 11, 2011

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Malfunction ·CORDIS DE MEXICO·Product code DTK·August 11, 2011