8,983 results · 43ms · Sources: EU EUDAMED, US FDA

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FDR GO

FDA Adverse Event
Injury ·SHIMADZU COPORATION·Product code IZL·July 1, 2025

LUPINE LOOP RAPIDE ANCHOR W/ORTHOCORD DS

FDA Adverse Event
Injury ·DEPUY MITEK LLC US·Product code MAI·June 28, 2019

MOTOBAND CP IMPLANT SYSTEM

FDA Adverse Event
Injury ·CROSSROADS EXTREMITY SYSTEMS LLC·Product code HRS·March 22, 2019

BIOKNOTLESS RC #2 ETHGR *EA

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·April 23, 2019

OMNISPAN MENISCAL REPAIR 27DEG

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·April 23, 2019

OMNISPAN MENISCAL REPAIR 27DEG

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·April 23, 2019

4.5 HEALIX BR ANCHOR W/ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·June 28, 2019

5.5 HEALIX TI ANCHR W/OC +NDLS

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MBI·September 9, 2019

LUPINE BR DS W/ORTHCRD

FDA Adverse Event
Injury ·DEPUY MITEK LLC US·Product code MAI·April 22, 2019

LUPINE BR DS W/ORTHCRD

FDA Adverse Event
Injury ·DEPUY MITEK LLC US·Product code MAI·April 22, 2019

DYNABUNION PLATE, 18MM, LEFT, STERILE

FDA Adverse Event
Injury ·SYNTHES TRAUMA : CROSSROADS EXTREMITY SYSTEMS, LLC·Product code HRS·December 27, 2022

5.5 HEALIX TI ANCHR W/OC +NDLS

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MBI·September 9, 2019

OMNISPAN MENISCAL REPAIR 27DEG

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·September 12, 2019

GRYPHON P BR DS ANCHOR W/OC

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·September 17, 2019

GRYPHON P BR DS ANCHOR W/ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·September 16, 2019

OMNISPAN MENISCAL REPAIR 12DEG

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·September 12, 2019

OMNISPAN MENISCAL REPAIR 12DEG

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·September 12, 2019

4.5 HEALIX TI ANCHOR W/OCORD

FDA Adverse Event
Injury ·DEPUY MITEK LLC US·Product code MBI·August 8, 2019

5.5MM HEALIX PEEK ANCHOR W/ORTHOCORD

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·August 28, 2019

MINI QUICKANCHOR® PLUS #2/0, SINGLE PACK

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code MAI·October 17, 2019