9 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SURGITEK BREAST IMPLANT
FDA Adverse Event
MEDICAL ENGINEERING CORP.·Product code FTR·February 17, 1994
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·July 14, 2024
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 13, 2024
CALCIUM
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code CJY·April 29, 2022
INSERTION HANDLE F/TROCHANTERIC FIXATION NAILS
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code FZX·March 12, 2013
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 17, 2011
EMBRACE PUMP
FDA Adverse Event
Malfunction
·ROSS PRODUCTS DIVISION·Product code LZH·February 18, 2008
C-TEK MAXAN ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·BIOMET SPINE - BROOMFIELD·Product code KWQ·November 12, 2015
C-TEK MAXAN ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·BIOMET SPINE - BROOMFIELD·Product code KWQ·November 12, 2015