26 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LANX SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EpiLong Paed
FDA UDI
Pajunk GmbH Medizintechnologie·14048223003104·EpiLong Paed
EPILONG
FDA UDI
Pajunk GmbH Medizintechnologie·04048223052372·0131156-51
3.5MM CORTEX SCREW SELF-TAPPING 55MM
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code HWC·January 26, 2017
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·July 25, 2018
SONOSITE EDGE ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
NAVITRACK SYSTEM-FLUOROSPINE, MODEL 900.005
FDA 510(k)
FDA Class 2
·Neurology
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·November 18, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·June 7, 2018
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
3.5MM CORTEX SCREW SELF-TAPPING 16MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 6, 2016
3.5MM CORTEX SCREW SELF-TAPPING 14MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 6, 2016
KANGAROO
FDA Adverse Event
Malfunction
·Product code LZH·May 15, 2013
ATTAIN OTW
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
UNKNOWN·Product code IKX·October 1, 2014
CORTSCR 3.5 SELF-TAP L65 TI
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code HWC·April 29, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 5, 2013
3.5MM CORTEX SCREW SELF-TAPPING 22MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·December 21, 2015