32 results · 23ms · 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.

GLUCOSE REAGENT FOR BECKMAN SYNCHRON CX & CX DELTA SYSTEMS

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Baltic Denture System BD Load

FDA UDI
Merz Dental GmbH·D7091033055·Baltic Denture System BDLoad ↓ Ln6 PLSEum4DFl D...

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0330150·Coronal Bender, Left

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0330050·Vise Grip, Large, 5.5mm

THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

MEDLINE STERILE POWDER FREE LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS)

FDA 510(k)
FDA Class 1 ·General Hospital

BI-METRIC LAT PC 13X145MM T1

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWZ·November 9, 2016

BI-METRIC LAT PC 12X140MM T1

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDI·November 9, 2016

BI-METRIC LAT PC 11X135MM T1

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDI·November 9, 2016

BI-METRIC LAT PC 10X130MM T1

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDI·November 9, 2016

BI-METRIC LAT PC 9X125MM T1

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWZ·November 9, 2016

SPIDERCUP

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code PBI·January 3, 2019

SPIDERCUP

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code PBI·January 3, 2019

UNKNOWN STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·November 9, 2018

RINGLOC MODULAR ACETABULAR SYSTEM

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code LPH·March 29, 2023

14X150MM BI-METRIC FEMORAL COLLARLESS STEM WITH TYPE 1 TAPER

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LPH·September 23, 2016

BI-METRIC FEMORAL COMPONENTS

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LPH·March 15, 2017

2800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 1, 2013

TRUFILL DCS ORBIT DETACHABLE COILS COMPLEX

FDA Adverse Event
Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code HCG·March 30, 2011

LIFEPAK CR PLUS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·April 23, 2008