1,270 results · 63ms · Sources: EU EUDAMED, US FDA

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MOSS GASTROSTOMY TUBE (5-17719)

FDA Adverse Event
Death ·MOSS TUBES, INC.·Product code KNT·November 4, 2015

MOSS GASTROSTOMY TUBE

FDA Adverse Event
Malfunction ·MOSS TUBES, INC.·Product code KNT·August 27, 2020

MOSS MIAMI SCREW

FDA Adverse Event
Injury ·DEPUY SYNTHES SPINE·Product code KWP·June 9, 2014

MOSS MIAMI SCREW

FDA Adverse Event
Injury ·DEPUY SYNTHES SPINE·Product code KWP·June 9, 2014

MOSS MIAMI SCREW

FDA Adverse Event
Injury ·DEPUY SYNTHES SPINE·Product code KWP·June 9, 2014

MOSS MIAMI SPINAL SYSTEM

FDA Adverse Event
Other ·DEPUY ACROMED, INC.·Product code KWQ·May 15, 2002

DERMABOND PRINEO 22CM MSH 3.8ML ADHESIVE

FDA Adverse Event
Injury ·ETHICON INC.·Product code OMD·February 8, 2022

UNKNOWN SCREW/ROD CONSTRUCT ACCESSORIES

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL CH·Product code MNH·December 23, 2019

UNKNOWN SCREWS

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL CH·Product code HWC·October 25, 2019

UNKNOWN SCREWS

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL CH·Product code HWC·October 25, 2019

UNKNOWN RODS

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL CH·Product code HSB·October 25, 2019

MOSS MIAMI SPINE SYSTEM HEXLOBE DRIVER 5.5 X25

FDA Adverse Event
Malfunction ·DEPUY SPINE INC·Product code HWR·October 24, 2023

UNK_THERMOCOOL SF NAV

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code LPB·November 26, 2025

THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

FDA Adverse Event
Death ·THORATEC CORPORATION·Product code DSQ·February 7, 2025

SURGIPRO

FDA Adverse Event
Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code FTL·December 7, 2021

UNKNOWN PALMAZ STENT

FDA Adverse Event
Death ·CORDIS CASHEL·Product code FGE·October 29, 2018

UNKNOWN SCREW/ROD CONSTRUCT ACCESSORIES

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SàRL CH·Product code MNH·December 10, 2019

MOSS MIAMI SPINE SYSTEM HEXLOBE DRIVER 5.5 X25

FDA Adverse Event
Malfunction ·DEPUY SPINE INC·Product code HWR·October 24, 2023

UNKNOWN PALMAZ STENT

FDA Adverse Event
Injury ·CORDIS CASHEL·Product code FGE·November 5, 2018

UNKNOWN PALMAZ STENT

FDA Adverse Event
Injury ·CORDIS CASHEL·Product code FGE·November 5, 2018