24 results · 26ms · Sources: EU EUDAMED, US FDA

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HEMOSIL D-DIMER

FDA 510(k)
FDA Class 2 ·Hematology

NOBELREPLACE CC PMC RP 4.3X10MM

FDA Adverse Event
Injury ·NOBEL BIOCARE USA INC·Product code DZE·June 15, 2021

NOBELPARALLEL CC NP 3.75X13MM

FDA Adverse Event
Injury ·NOBEL BIOCARE AB·Product code DZE·March 8, 2021

NOBELPARALLEL CC NP 3.75X13MM

FDA Adverse Event
Injury ·NOBEL BIOCARE AB·Product code DZE·March 8, 2021

V/X ASPHERIC TORIC MULTIFOCAL (POLYMACON) SOFT (HYDROPHILIC) LENSES WITH A CLEAR OR BLUE VISIBILITY TINT

FDA 510(k)
FDA Class 2 ·Ophthalmic

DISCOVERY ELBOW

FDA 510(k)
FDA Class 2 ·Orthopedic

LINEAR ST

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 20, 2023

KIT IMPLANTABLE SLIM TIP LEAD, 50CM

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code PMP·November 15, 2022

UNKNOWN KUDO ELBOW

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

Integra Cranial access kit (without Prep solutions) Bit and Guard-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: INS5HND

FDA Enforcement
Class II ·Ongoing·Integra LifeSciences Corp.·December 13, 2023

DISC LT DSTL HMRL BDY SET

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDC·April 1, 2019

UNKNOWN KUDO ELBOW

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

UNKNOWN KUDO ELBOW

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

UNKNOWN KUDO ELBOW

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

UNKNOWN KUDO ELBOW

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

UNKNOWN KUDO ELBOW

FDA Adverse Event
Death ·BIOMET UK LTD.·Product code JDC·May 19, 2017

UNKNOWN KUDO ELBOW

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

ADVANTAGE SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·April 23, 2013

GOBED+

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·April 21, 2011

RIATA ST OPTIM ACTIVE FIXATION

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