17 results · 31ms · Sources: EU EUDAMED, 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