7,293 results · 38ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

AESCULAP PRESTIGE GRASPER

FDA Adverse Event
Injury ·AESCULAP, INC.·Product code NWV·August 24, 2023

AMS INFLATABLE PENILE PROSTHESIS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FHW·June 3, 2020

STEFFEE PLATE AND SCREW

FDA Adverse Event
ACROMED CORP.·Product code MCV·April 24, 1995

SURGITEK GEL-FILLED MAMMARY IMPLANT

FDA Adverse Event
Injury ·MEDICAL ENGINEERING CORP.·Product code FTR·May 19, 1995

ADVANTAGE TRANSVAGINAL MID-URETHRAL SLING SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FTL·April 22, 2019

EXCIMER, LASER SYSTEM

FDA Adverse Event
Injury ·UNK·Product code LZS·May 9, 2019

*

FDA Adverse Event
Injury ·*·Product code HQL·November 24, 2006

SHWERWOOD

FDA Adverse Event
Injury ·THE KENDALL CO. LP·Product code KNT·February 9, 2000

HEMASHIELD KNITTED DOUBLE VELOUR FABRIC

FDA Adverse Event
Injury ·MEADOX MEDICAL, INC., DIV. B.S.C.·Product code DXZ·March 21, 1997

CENTRAX BIPOLAR PROSTHESIS 57MM X 26MM

FDA Adverse Event
Injury ·HOWMEDICA, INC.·Product code MJT·August 31, 1994

MENTOR

FDA Adverse Event
Other ·MENTOR·Product code FTR·February 7, 2005

SELOX ST 60

FDA Adverse Event
Malfunction ·BIOTRONIK GMBH AND CO.·Product code DXY·August 9, 2007

MENTOR SALINE SMOOTH ROUND

FDA Adverse Event
Injury ·MENTOR·Product code FWM·August 21, 2018

SYNVISC ONE

FDA Adverse Event
Injury ·GENZYME CORPORATION·Product code MOZ·August 7, 2018

FILSHIE CLIP

FDA Adverse Event
Injury ·UNK·Product code KNH·August 7, 2018

ADVANCED MEDICAL OPTICS INC

FDA Adverse Event
Other ·ADVANCED MEDICAL OPTICS, INC·Product code LPN·May 28, 2007

GEL-FILLED MAMMARY IMPLANT

FDA Adverse Event
Injury ·DOW CORNING CORP.·Product code FTR·September 25, 1995

ESSURE

FDA Adverse Event
Injury ·BAYER HEALTHCARE LLC·Product code HHS·January 14, 2020

LASER DEVICE USED FOR TURP PROCEDURE

FDA Adverse Event
Injury ·*·Product code LNK·June 7, 2002

MENTOR SALINE BREAST IMPLANTS

FDA Adverse Event
Injury ·MENTOR·Product code FWM·January 19, 2018