17 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KLOCKNER DENTAL IMPLANT ABUTMENTS (II)
FDA 510(k)
FDA Class 2
·Dental
AGXO
FDA UDI
Oticon A/S·05707131280183·H110, DESIGNRITE 10 WL MIBU AGXO
1.5MM SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036032432·
NAVIGATOR DELIVERY SYSTEM (OR NAVIGATOR DS) MODEL: NAV-010
FDA 510(k)
FDA Class 2
·General Hospital
BD ONECATH PERIPHERALLY INSERTED CENTRAL CATHETER, MODELS 384647, 384667, 384687, 384648, 384668, 384688, 384649, 384669
FDA 510(k)
FDA Class 2
·General Hospital
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013
VIPER2 SET SCREW INSERTER, SELF-RETAINING
FDA Adverse Event
Malfunction
·DEPUY SPINE, INC.·Product code LXH·June 21, 2011
SPRINT FIDELIS
FDA Adverse Event
Malfunction
·MEDTRONIC, INC. CARDIAC RHYTHM DISEASE MGMT.·Product code LWS·August 12, 2008
PIPELINE
FDA Adverse Event
Death
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·April 18, 2024
REFLEX CATHETER
FDA Adverse Event
Death
·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·April 18, 2024
UNKNOWN SOLITAIRE
FDA Adverse Event
Death
·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·April 18, 2024
PIPELINE
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·April 18, 2024
UNKNOWN SOLITAIRE
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·April 18, 2024
REFLEX CATHETER
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·April 18, 2024
1.5MM SYSTEM HIGH TORQUE X-LOCK STANDARD BLADE
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code JEY·October 18, 2018
RESTORE SENSOR
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·August 31, 2016
BIOMET MICROFIXATION FACIAL PLATING SYSTEM
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code JEY·May 3, 2017