3,466 results · 26ms · Sources: EU EUDAMED, US FDA

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PENTAX PNE- ULTRA-SLIM UPPER G.I. FIBERSCOPE FG-23

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

VAGISPEC KOLPLAST

FDA UDI
Kolplast C I·07898027905988·

VERIFY ENHANCED

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·March 30, 2021

VERIFY ENHANCED

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·July 2, 2018

INTERSTIM II

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·March 26, 2015

SACRAL NERVE IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·February 24, 2010

SACRAL NERVE IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MQQ·February 24, 2010

SACRAL NERVE IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·February 24, 2010

INTERSTIM IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MQQ·February 24, 2010

INTERSTIM

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·April 8, 2021

AXONICS

FDA Adverse Event
Injury ·AXONICS, INC·Product code EZW·December 19, 2024

INTERSTIM

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·October 16, 2014

INTERSTIM

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·October 16, 2014

AXONICS

FDA Adverse Event
Malfunction ·AXONICS MODULATION TECHNOLOGIES, INC.·Product code EZW·February 6, 2020

INTERSTIM

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·January 6, 2012

AXONICS

FDA Adverse Event
Malfunction ·AXONICS MODULATION TECHNOLOGIES, INC.·Product code EZW·February 1, 2020

AXONICS

FDA Adverse Event
Injury ·Product code EZW·August 27, 2020

IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·November 16, 2020

EXTERNAL NEUROSTIMULATOR, UNKNOWN

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·April 23, 2014

VERIFY ENHANCED

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·October 4, 2022