18 results · 26ms · Sources: EU EUDAMED, US FDA

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ZMI Self-Adhesive Electrodes

FDA 510(k)
FDA Class 2 ·Neurology

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·October 9, 2009

AVA NAVIGATOR PEEK SPACERS, MODEL 48392XXX, 48393XXX

FDA 510(k)
FDA Class 2 ·Orthopedic

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA 510(k)
FDA Class 2 ·General Hospital

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·July 20, 2009

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·October 9, 2009

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

TITAN TOUCH

FDA Adverse Event
Injury ·COLOPLAST A/S·Product code FHW·July 6, 2021

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·October 26, 2010

FREESTYLE FREEDOM

FDA Adverse Event
Injury ·Product code NBW·June 20, 2013

DUAL COOLER/HEATER

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWC·July 1, 2011

RESTORE PRIME ADVANCED

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·September 23, 2008

DIVA

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

DIVA

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

SENRI

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code DQY·December 25, 2016

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·July 20, 2009

METACROSS RX PTA BALLOON DILATATION CATHETER

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·October 15, 2019