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

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SPIRA-C Open Matrix Cervical Interbody

FDA 510(k)
FDA Class 2 ·Orthopedic

OsteoMed

FDA UDI
OSTEOMED LLC·00845694027335·2.4mm X 46mm Cannulated Headless Screw

OsteoMed

FDA UDI
OSTEOMED LLC·00845694069144·Cannulated 2.4 x 46mm Headless Screw Sterile Qty 2

TOMOTHERAPY TREATMENT SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

MOBIL-O-GRAPH NG 24 H ABP-CONTROL

FDA 510(k)
FDA Class 2 ·Cardiovascular

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·October 17, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·November 9, 2018

ROSA ONE

FDA Adverse Event
Injury ·MEDTECH SA·Product code HAW·January 11, 2019

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 3, 2025

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code NAY·January 21, 2019

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·December 21, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

ARCOM 28MM RNGLOC LNR 10DEG24

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code LPH·June 17, 2013

TOTALCARE BED

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·June 17, 2011

ROTABLATOR GUIDE WIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code MCX·September 19, 2008

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018