1,193 results · 36ms · Sources: EU EUDAMED, US FDA

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OOSTEOTITE BONE SCREW 200/50 MM SHAFT D 6 MM

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code HWC·March 5, 2013

HANDSET FOR OSCAR II

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code JDX·March 27, 2018

COMPRESSION DISTRACTION UNIT LONG

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code JDW·December 2, 2019

COMPRESSION DISTRACTION UNIT LONG

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code JDW·December 2, 2019

COMPRESSION DISTRACTION UNIT LONG

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code JDW·December 2, 2019

FITBONE INTRAMEDULLARY LENGTHENING NAIL TAA1180-F-245

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code HSB·September 14, 2023

ROD CLIP CLAMP

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code JDW·January 24, 2020

RADIOLUCENT HANDLE

FDA Adverse Event
Malfunction ·ORTHOFIX SRL·Product code HSB·November 5, 2015

XCALIBER OSTEOTITE SCREW L 150/30 MM THREAD D 6.0-5.6MM

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code JDW·May 5, 2020

EIGHT-PLATE GUIDED GROWTH PLATE 16MM

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code HRS·August 1, 2022

CENTRONAIL TITANIUM TIBIAL NAIL D.8 MM-L.305 MM

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code HSB·August 23, 2022

EIGHT-PLATE GUIDED GROWTH PLATE 16MM

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code HRS·August 1, 2022

TRUE LOK WIRE

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code KTT·November 23, 2016

PAEDIATRIC LRS C/D UNIT EXTENDS TO 6.2 CM

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code JDW·June 21, 2017

STRAIGHT CLAMP FOR PAEDIATRIC LRS

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code JDW·June 21, 2017

STRAIGHT CLAMP FOR PAEDIATRIC LRS

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code JDW·June 21, 2017

XCALIBER OSTEOTITE SCREW L 150/30 MM THREAD D 6.0-5.6MM

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code JDW·March 13, 2020

EIGHT-PLATE GUIDED GROWTH PLATE 12MM

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code HRS·August 1, 2022

XCALIBER ARTICULATED ANKLE KIT STERILE

FDA Adverse Event
Malfunction ·ORTHOFIX SRL·Product code JDW·December 10, 2013

ADV LRS KIT 300MM

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code JDW·May 7, 2024