2,469 results · 29ms · Sources: EU EUDAMED, US FDA

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Vista Ankle Hydraulic

FDA UDI
CYPRESS ADAPTIVE, LLC·00850013242290·Hydraulic ankle for elevated vacuum suspension

iNSitu Hip System

FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127027260·Broach Extraction Handle, Small

TOTALCARE

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·January 13, 2012

PT,TABLE,CRANK HYD,CUBBY,48x30X26-36"

FDA UDI
Hausmann Enterprises, LLC·00840314803221·

PT,TABLE,CRANK HYD,CONVERT,78x36X30-40

FDA UDI
Hausmann Enterprises, LLC·00840314802927·

TRANSPORT SERIES OBS10/25/04

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FPO·May 27, 2011

TOTALCARE

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·February 3, 2011

CYPHER SIROLIMUS-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code NIQ·April 12, 2006

TOTALCARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·April 12, 2010

THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

FDA Adverse Event
Injury ·THORATEC CORPORATION·Product code DSQ·June 28, 2024

LIFTER

FDA Adverse Event
Other ·SUNRISE MEDICAL·Product code FNJ·November 4, 2000

HOYER LIFTER

FDA Adverse Event
Other ·APEX HEALTHCARE MFG INC·Product code FSA·June 26, 2006

CYPHER SIROLIMUS-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code NIQ·August 1, 2005

HOYER LIFTER

FDA Adverse Event
Other ·APEX HEALTHCARE MFG INC·Product code FNG·August 7, 2006

SYNCHROMED II

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·July 30, 2021

HOYER LIFT

FDA Adverse Event
Other ·APEX HLTHCARE MFG INC·Product code FSA·June 26, 2006

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·May 11, 2021

WAVELIGHT FS200 FEMTOSECOND LASER

FDA Adverse Event
Injury ·WAVELIGHT GMBH·Product code GEX·October 31, 2025

BARD® INLAY OPTIMA® URETERAL STENT

FDA Adverse Event
Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FAD·November 7, 2021

PRECISE OTW NITINOL STENT

FDA Adverse Event
Death ·CORDIS DE MEXICO·Product code NIM·August 4, 2009