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

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MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7 MM; MICRUS ASCENT OCCLUSION BALLOON CATHETER 6X9 MM; MICRUS SUMMIT OCCLUSIO

FDA 510(k)
FDA Class 2 ·Cardiovascular

FEEDING/DOSING CANNULA

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896091092·FEEDING/DOSING CANNULA CURVED BALL TIP

VITAL SUTURES, SUTUREX, CIRUGIA PERUANA

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

VERTEX RECONSTRUCTION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

REVERSE SHOULDER SYSTEM HUMERAL REVERSE METAPHYSIS +0MM/0°

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·July 26, 2023

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·January 26, 2012

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·January 26, 2012

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·October 15, 2009

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·December 31, 2009

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·October 29, 2009

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 9, 2013

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·September 19, 2014

PARADIGM INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code LZG·May 18, 2011

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 21, 2010

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 21, 2010

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·August 13, 2010

FIAB EURODEFIPADS

FDA Adverse Event
Malfunction ·FIAB S.P.A.·Product code LDD·October 19, 2022

EURODEFIPADS

FDA Adverse Event
Malfunction ·FIAB SPA·Product code LDD·April 19, 2023

DEFICOM

FDA Adverse Event
Malfunction ·FIAB SPA·Product code LDD·December 21, 2023

SHOULDER SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·February 6, 2025