13 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODELS 27040 & 27050 CONTI. FLOW RESECTOSCOPES
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Cellene CO2 Laser System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OCTANE VERTEBRAL BODY REPLACEMENT (VBR) SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
RESTORE ADVANCED
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·February 4, 2015
PISCES-QUAD
FDA Adverse Event
Injury
·NEURO - VILLALBA·Product code LGW·November 30, 2015
PISCES-QUAD
FDA Adverse Event
Injury
·NEURO - VILLALBA·Product code LGW·November 30, 2015
RESTORE SENSOR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 15, 2013
SIG PS CEM FEM W/LUGS RT SZ3
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS 121965·Product code NJL·June 18, 2014
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·October 20, 2010
FUSION NAVIGATION SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·December 20, 2012
3.2MMX40MM RNGLC+ ACET DRL BIT
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code HTW·September 3, 2021
RESTORE SENSOR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 7, 2015
RESTORE ADVANCED
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 23, 2013