114 results · 78ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

CUSTOM SPINE, INC.

FDA Adverse Event
Injury ·CUSTOM SPINE, INC.·Product code LXH·February 5, 2010

ISSYS PEDICLE SCRE SYSTEM

FDA Adverse Event
Other ·CUSTOM SPINE, INC.·Product code KWP·April 3, 2012

ISSYS PEDICLE SCREW 6.5 MM X 50 MM

FDA Adverse Event
Malfunction ·CUSTOM SPINE, INC.·Product code MCV·November 26, 2008

06.5MM ISSYS PEDICLE SCREW SYSTEM

FDA Adverse Event
Malfunction ·CUSTOM SPINE, INC.·Product code MCV·June 22, 2006

ISSYS PEDICLE SCREW

FDA Adverse Event
Other ·CUSTOM SPINE, INC.·Product code MCV·February 25, 2008

ISSYS LP SPINAL SCREW

FDA Adverse Event
Malfunction ·CUSTOM SPINE, INC.·Product code NKB·July 2, 2010

OPTRELL

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DRF·August 13, 2025

PENTARAY NAV HIGH-DENSITY MAPPING ECO CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC.·Product code MTD·February 25, 2019

PENTARAY NAV HIGH-DENSITY MAPPING ECO CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code MTD·June 8, 2024

PENTARAY NAV

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code MTD·September 23, 2024

PENTARAY NAV ECO HIGH-DENSITY MAPPING CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code MTD·October 25, 2016

PENTARAY NAV HIGH-DENSITY MAPPING ECO CATHETER

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC.·Product code MTD·October 31, 2018

FLEXTIP PLUS CLOSED-TIP MULTIPORT EPIDURAL CAT

FDA Adverse Event
Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·October 3, 2017

OCTARAY MAPPING CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code MTD·October 27, 2023

OCTARAY MAPPING CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code MTD·December 18, 2025

VIZIGO

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·March 26, 2025

CITADEL

FDA Adverse Event
Malfunction ·ARJOHUNTLEIGH POLSKA·Product code FNL·October 2, 2017

PENTARAY NAV HIGH-DENSITY MAPPING ECO CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code MTD·January 12, 2023

PENTARAY NAV HIGH-DENSITY MAPPING ECO CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code MTD·May 19, 2021

PENTARAY NAV HIGH-DENSITY MAPPING CATHETER

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code MTD·October 13, 2022