67 results · 24ms · Sources: EU EUDAMED, US FDA

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SATURNO(TM) OVERDENTURE IMPLANT SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

ABCFlex™, ABC®

FDA UDI
Conmed Corporation·30653405043434·ABCFlex™, ABC® Flexible Endoscopy Probe 2.3 mm ...

HHM

FDA UDI
Oticon A/S·05707131260260·H100, MINIBTE 312 WL 85 SGR HHM

HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

DISCOVERY MR750W 3.0T

FDA 510(k)
FDA Class 2 ·Radiology

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·July 22, 2015

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·June 18, 2015

PENUMBRA SYSTEM JETD REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·May 8, 2019

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·July 17, 2015

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·October 30, 2015

PENUMBRA SYSTEM 3MAX REPERFUSION CATHETER

FDA Adverse Event
Injury ·PENUMBRA, INC.·Product code NRY·June 14, 2015

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·June 26, 2015

OCTRODE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 20, 2013

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

SWAN-GANZ CCO

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES·Product code DYG·June 13, 2011

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·June 9, 2015

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·September 9, 2015

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·September 16, 2015

PENUMBRA SYSTEM 4MAX REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·July 30, 2015

PENUMBRA SYSTEM JETD REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·November 11, 2021