31 results · 39ms · Sources: EU EUDAMED, US FDA

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YUKON OCT Spinal System

FDA 510(k)
FDA Class 2 ·Orthopedic

VeriQuick

FDA UDI
FOURSTAR GROUP INC.·00049696609531·

Ambler Value Line

FDA UDI
AMBLER SURGICAL CORP.·00190660214210·Deaver retractor, 12'' long x 2'' wide blade, f...

MECHANICAL WHEELCHAIR - L-FRAME SERIES

FDA 510(k)
FDA Class 1 ·Physical Medicine

AUTOSUTURE ENDO GIA SINGLE USE TAN RELOAD WITH TRI-STAPLE TECHNOLOGY

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

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

INCORPORATE

FDA UDI
SPINAL ELEMENTS·00840606151979·17 X 14 CERVICAL TRIALS 44MM 0° LORDOSIS

INCORPORATE

FDA UDI
SPINAL ELEMENTS·00840606152167·17 X 14 CERVICAL TRIALS 44MM 10° LORDOSIS

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

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

VC10 PUMP, 115V

FDA Adverse Event
Malfunction ·GYRUS ACMI, INC.·Product code HHK·January 2, 2025

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 15, 2013

COMMUNICATOR

FDA Adverse Event
Malfunction ·EXTERNAL MANUFACTURER·Product code LWS·July 21, 2011