26 results · 20ms · Sources: EU EUDAMED, 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