14 results
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40ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
FACETCORESYSTEM
FDA Adverse Event
Malfunction
·SURGENTEC, LLC·Product code MDM·November 9, 2021
TILINK-P SI JOINT FUSION SYSTEM
FDA Adverse Event
Injury
·SURGENTEC, LLC·Product code OUR·September 30, 2024
FACETCORE SYSTEM
FDA Adverse Event
Malfunction
·SURGENTEC, LLC·Product code MDM·December 2, 2020
BMAN SOLID DIAMOND NEEDLE
FDA Adverse Event
Malfunction
·SURGENTEC, LLC·Product code KNW·October 9, 2025
FACETCORE SYSTEM
FDA Adverse Event
Malfunction
·SURGENTEC, LLC·Product code MDM·November 9, 2021
3D GRAFTRASP SYSTEM
FDA Adverse Event
Malfunction
·SURGENTEC, LLC·Product code FMF·July 29, 2021
ALARA ACCESS NEEDLE
FDA Adverse Event
Malfunction
·SURGENTEC, LLC·Product code GDF·June 6, 2019
TILINK - P
FDA Adverse Event
Injury
·SURGENTEC, LLC·Product code OUR·August 5, 2024
TILINK-P SI JOINT FUSION SYSTEM
FDA Adverse Event
Malfunction
·SURGENTEC, LLC·Product code OUR·September 30, 2024
FACETCORE SYSTEM
FDA Adverse Event
Malfunction
·SURGENTEC, LLC·Product code MDM·June 2, 2023
ALARA NEURO ACCESS NEEDLE
FDA Adverse Event
Malfunction
·SURGENTEC, LLC·Product code PDQ·May 14, 2025
TILINK-P SCREW 12MM X 25MM
FDA Adverse Event
Death
·SURGENTEC, LLC·Product code OUR·May 14, 2025
GRAFTGUN CARTRIDGE KT
FDA Adverse Event
Malfunction
·SURGENTEC, LLC·Product code FMF·February 25, 2025
BMAN SOLID DIAMOND NEEDLE
FDA Adverse Event
Malfunction
·SURGENTEC, LLC·Product code KNW·March 18, 2026