61 results · 27ms · Sources: EU EUDAMED, US FDA

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UNK - CONSTRUCTS: PFNA-II

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code HSB·July 15, 2021

UNK - CONSTRUCTS: PFNA

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code HSB·March 7, 2021

INSULIN REPOSITORY

FDA Adverse Event
DISETRONIC MEDICAL SYSTEMS·Product code LZG·September 17, 1998

ENDOTAK DSP

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS·Product code LWS·February 9, 2001

DURATA STS OPTIM

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 11, 2008

DURATA STS OPTIM ACTIVE FIXATION LEAD, DF-4 CONNECTO

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2012

GUGLIELMI DETACHABLE COIL- GDC-10

FDA Adverse Event
Malfunction ·TARGET THERAPEUTICS/A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code HCG·March 16, 1999

SWEET TIP BIPOLAR LEAD

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS·Product code DXY·July 8, 1997

BIPOLAR STEROID ELUTING LEAD

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS·Product code DTB·May 8, 1997

INFLATABLE PENILE PROSTHESIS

FDA Adverse Event
Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FHW·January 2, 1997

ENDOTAK RELIANCE

FDA Adverse Event
Malfunction ·CPI - DEL CARIBE·Product code LWS·April 2, 2015

MOBILE STAND

FDA Adverse Event
Malfunction ·CRITIKON, DIV OF ETHICON, INC.·Product code DXN·July 10, 1998

PRECISION

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·June 11, 2009

ENDOTAK RELIANCE G

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·August 9, 2006

ACUITY

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code OJX·April 11, 2013

SWEET TIP BIPOLAR LEAD

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS·Product code DXY·March 6, 1997

IMPLANTABLE COLLAMER LENS (ICL)

FDA Adverse Event
Malfunction ·STAAR SURGICAL COMPANY·Product code MTA·March 23, 2024

IMPLANTABLE DEFIBRILLATOR/PACEMAKER/LEAD

FDA Adverse Event
CARDIAC PACEMAKERS, INC.·Product code LWS·January 31, 1996

ACCLAIM STANDARD TUBING DEVICE

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code FRN·April 17, 1998

TI MATRIXMIDFACE SCREW SELF-DRILLING 6MM

FDA Adverse Event
Malfunction ·SYNTHES MONUMENT·Product code DZL·April 27, 2017