10,000 results · 253ms · Sources: EU EUDAMED, US FDA

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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