134 results · 42ms · Sources: EU EUDAMED, US FDA

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OPTILIF AND OPTIMESH

FDA Adverse Event
Injury ·SPINEOLOGY INC.·Product code OQB·January 31, 2025

PALISADE PEDICULAR FIXATION SYSTEM

FDA Adverse Event
Malfunction ·SPINEOLOGY INC.·Product code NKB·October 11, 2016

RAMPART-O 30X8

FDA Adverse Event
Malfunction ·SPINEOLOGY INC.·Product code MAX·December 15, 2016

OPTIMESH

FDA Adverse Event
Malfunction ·SPINEOLOGY, INC.·Product code EZX·February 27, 2009

OPTIMESH

FDA Adverse Event
Injury ·SPINEOLOGY, INC.·Product code EZX·January 4, 2010

OPTIMESH

FDA Adverse Event
Injury ·SPINEOLOGY, INC.·Product code EZX·January 4, 2010

KIT, SURGICAL INSTRUMENT, DISPOSABLE

FDA Adverse Event
Malfunction ·SPINEOLOGY, INC.·Product code KDD·April 21, 2021

OPTIMESH 1500 E

FDA Adverse Event
Malfunction ·SPINEOLOGY, INC·Product code EZX·November 19, 2021

ELITE EXPANDABLE INTERBODY FUSION DEVICE

FDA Adverse Event
Injury ·SPINEOLOGY, INC·Product code MAX·April 12, 2022

OPTIMESH

FDA Adverse Event
Other ·SPINEOLOGY, INC.·Product code FTL·February 7, 2012

PALISADE

FDA Adverse Event
Injury ·SPINEOLOGY INC.·Product code NKB·July 10, 2024

PALISADE

FDA Adverse Event
Injury ·SPINEOLOGY INC.·Product code NKB·July 10, 2024

PALISADE

FDA Adverse Event
Injury ·SPINEOLOGY INC.·Product code NKB·July 10, 2024

PALISADE

FDA Adverse Event
Injury ·SPINEOLOGY INC.·Product code NKB·July 10, 2024

PALISADE

FDA Adverse Event
Injury ·SPINEOLOGY INC.·Product code NKB·July 10, 2024

GRAFT TUBE

FDA Adverse Event
Malfunction ·SPINEOLOGY INC.·Product code LXH·August 27, 2024

PALISADE

FDA Adverse Event
Injury ·SPINEOLOGY INC.·Product code NKB·July 10, 2024

OPTIMESH

FDA Adverse Event
Other ·SPINEOLOGY, INC.·Product code EZX·November 17, 2008

OPTIMESH

FDA Adverse Event
Other ·SPINEOLOGY, INC.·Product code EZX·November 17, 2008

OPTIMESH

FDA Adverse Event
Injury ·SPINEOLOGY INC.·Product code OQB·October 1, 2025