41 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·July 11, 2017
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·September 3, 2019
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL·Product code MAI·September 3, 2019
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·November 29, 2018
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·October 3, 2018
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·July 6, 2020
M2A 38MM MOD HD -6MM NK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·October 29, 2014
MEDISENSE OPTIUM
FDA Adverse Event
Malfunction
·Product code NBW·August 12, 2011
VITALITY 2
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 8, 2013
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 5, 2025
L3C0600 - CURE PRODUCTS
FDA Adverse Event
Malfunction
·CONVATEC INC·Product code GBM·July 19, 2022
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·March 14, 2019
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code MAI·March 14, 2019
GRYPHON BR ANCHOR W/ PROKNOT TECHNOLOGY
FDA Adverse Event
Injury
·DEPUY MITEK·Product code MAI·March 16, 2017
GRYPHON P BR DS ANCHOR W/ORTHOCORD
FDA Adverse Event
Injury
·DEPUY MITEK·Product code MAI·March 16, 2017
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·August 24, 2018
GRYPHON ORTHOCORD
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·April 9, 2026
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·January 25, 2019
GRYPHON P BR DS ANCHOR W/OC
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·January 14, 2019
GRYPHON ORTHOCORD
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code MAI·April 8, 2026