25 results · 28ms · Sources: EU EUDAMED, US FDA

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LaborView LV1000

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

MUCHECK, VERSION 9.0

FDA 510(k)
FDA Class 2 ·Radiology

CALC-I-OSS

FDA 510(k)
FDA Class 2 ·Dental

WAVEWRITER ALPHA? 16

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 15, 2025

BD SYRINGE LUER-LOK TIP

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 21, 2019

UNKNOWN BI-METRIC POROUS PRIMARY HIP

FDA Adverse Event
Death ·ZIMMER BIOMET, INC.·Product code LPH·October 11, 2017

SYNCHROMED II

FDA Adverse Event
Injury ·RICE CREEK MFG·Product code LKK·June 3, 2013

TOTALCARE BARIATRIC

FDA Adverse Event
Malfunction ·HILL-ROM INC.·Product code FNL·June 21, 2011

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

UNKNOWN ALLIANCE REVISION HIP SYSTEMS

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 11, 2017

UNKNOWN ALLIANCE REVISION HIP SYSTEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 11, 2017

UNKNOWN ALLIANCE REVISION HIP SYSTEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 11, 2017

UNKNOWN BI-METRIC POROUS PRIMARY HIP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 10, 2017

ALLIANCE REVISION HIP SYSTEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 10, 2017

UNKNOWN BI-METRIC POROUS PRIMARY HIP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 10, 2017

UNKNOWN ALLIANCE REVISION HIP SYSTEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 10, 2017

UNKNOWN ALLIANCE REVISION HIP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 11, 2017

UNKNOWN ALLIANCE REVISION HIP SYSTEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 10, 2017

UNKNOWN ALLIANCE REVISION HIP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·October 10, 2017

UNKNOWN ALLIANCE REVISION HIP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 22, 2017