10,000 results
·
253ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
IMPLANET SPINE SYSTEM
FDA Adverse Event
Malfunction
·IMPLANET·Product code NKB·July 22, 2016
INFLATABLE PENILE PROSTHESIS
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FHW·July 11, 1997
JAZZ LOCK
FDA Adverse Event
Injury
·IMPLANET·Product code OWI·November 24, 2017
JAZZ
FDA Adverse Event
Malfunction
·IMPLANET·Product code OWI·February 7, 2017
IMPLANET SPINE SYSTEM
FDA Adverse Event
Malfunction
·IMPLANET·Product code NKB·February 25, 2016
IMPLANET SPINE SYSTEM
FDA Adverse Event
Malfunction
·IMPLANET·Product code NKB·December 22, 2016
JAZZ SYSTEMS
FDA Adverse Event
Injury
·IMPLANET·Product code OWI·June 12, 2017
JAZZ LOCK
FDA Adverse Event
Malfunction
·IMPLANET·Product code OWI·February 16, 2026
JAZZ LOCK
FDA Adverse Event
Malfunction
·IMPLANET·Product code OWI·February 16, 2026
JAZZ LOCK
FDA Adverse Event
Malfunction
·IMPLANET·Product code OWI·February 16, 2026
IMPLANET SPINE SYSTEM
FDA Adverse Event
Injury
·IMPLANET·Product code NKB·June 24, 2015
JAZZ
FDA Adverse Event
Injury
·IMPLANET·Product code OWI·March 19, 2020
SCREW-VENT DENTAL IMPLANT
FDA Adverse Event
Injury
·CORE-VENT BBIO-ENGINEERING·Product code DZE·December 23, 1994
SCREW-VENT DENTAL IMPLANT
FDA Adverse Event
Injury
·CORE-VENT BIO ENGINEERING·Product code DZE·May 2, 1994
GEL MAMMARY PROSTHESIS
FDA Adverse Event
Injury
·AMERICAN HEYER SCHULTE·Product code FTR·March 17, 1997
COLLAMER LENS
FDA Adverse Event
Injury
·STAAR SURGICAL·Product code HQL·October 24, 2001
CORE-VENT IMPLANAT
FDA Adverse Event
Injury
·COREVENT CORPORATION·Product code DZE·April 5, 1993
ELASTIMIDE FOLDABLE SILICONE POSTERIOR CHAMBER INTRAOCULAR L
FDA Adverse Event
Injury
·STAAR SURGICAL CO.·Product code HQL·April 27, 2005
CONTAK RENEWAL
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·August 9, 2006
ELASTIC LENS
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code HQL·January 13, 1999