15 results · 23ms · Sources: EU EUDAMED, US FDA

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RENALIN

FDA Adverse Event
Other ·MINNTECH CORP.·Product code LIF·April 4, 1994

TUFF IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·April 16, 2026

TUFF IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·January 27, 2026

TUFF IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·February 24, 2026

TUFF IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·November 6, 2025

NEURON MAX 6F 088 LONG SHEATH

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DQY·February 10, 2016

NEURON MAX 6F 088 LONG SHEATH

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code DQY·February 10, 2016

EXODONTIA ELEVATOR #46R SERRATED

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code EMJ·March 29, 2016

OCTRODE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·March 5, 2013

HEARTMATE II SYSTEM CONTROLLER

FDA Adverse Event
Malfunction ·THORATEC CORPORATION·Product code DSQ·January 26, 2011

EAGLE EYE CATHETER

FDA Adverse Event
Other ·VOLCANO CORPORATION·Product code DQO·February 20, 2008

EXODONTIA ELEVATOR #46R SERRATED

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code EMJ·March 29, 2016

EXODONTIA ELEVATOR #46R SERRATED

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code EMJ·March 29, 2016

ANCHOR BOLTS

FDA Adverse Event
Malfunction ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·May 17, 2019

MI-750

FDA Adverse Event
Malfunction ·MEDICAL ILLUMINATION INTRNATION INC.·Product code FSY·January 17, 2023