63 results
·
38ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TELEGRAPH EVO
FDA Adverse Event
Malfunction
·FH INDUSTRIE·Product code HSB·August 26, 2025
LGN PS HIGH FLEX XLPE SZ 5-6 9MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·September 1, 2016
SCORPIO NRG CR FEMORAL COMPONENT RIGHT #7
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·February 7, 2013
BOLERO
FDA Adverse Event
Injury
·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·August 30, 2023
MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·January 27, 2015
UNKNOWN HIP FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·September 25, 2023
TOUCH CMC 1 PROSTHESIS
FDA Adverse Event
Injury
·KERI MEDICAL SA·Product code SFA·November 7, 2025
VIBRANT SOUNDBRIDGE
FDA Adverse Event
Malfunction
·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MPV·March 13, 2023
TRANSFER BENCH
FDA Adverse Event
Injury
·MEDLINE INDUSTRIES, INC.·Product code ILS·September 5, 2014
UNKNOWN HIP FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·September 27, 2023
UNKNOWN HIP FEMORAL STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·September 25, 2023
UNKNOWN HIP ACETABULAR LINERS
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·September 25, 2023
UNK HIP ACETABULAR CUP PINNACLE
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·September 25, 2023
CLAREON VIVITY EXTENDED VISION UV ABSORBING IOL
FDA Adverse Event
Injury
·ALCON LABORATORIES IRELAND LTD.·Product code POE·January 5, 2026
UNKNOWN ILIZAROV EXFIX DEVICE
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JDW·May 6, 2020
UNKN ILIZAROV EXFIX DEV
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JDW·May 6, 2020
ZILVER PTX 35 DRUG-ELUTING STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code NIU·November 22, 2018
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·October 5, 2020
TOTAL KNEE REPLACEMENT (REVISION)
FDA Adverse Event
Injury
·STANMORE IMPLANTS WORLDWIDE·Product code KRO·October 3, 2019
LCP(TM) DISTAL FEMUR PLATE 9 HOLES/236MM-RIGHT
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HRS·March 5, 2024