16 results
·
55ms
·
Sources: EU EUDAMED, US FDA
NEXUS SPINE, LLC.
FDA registration
NEXUS SPINE, LLC.·12 products·🇺🇸 United States
NEXUS® BONESCALPEL® 25MM, BLUNT BLADE + IRRIGATION TUBING KIT
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·November 13, 2024
NEXUS® ULTRASONIC SURGICAL ASPIRATOR SYSTEM
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·November 10, 2023
NEXUS® ULTRASONIC SURGICAL ASPIRATION SYSTEM
FDA Adverse Event
Injury
·MISONIX, INC.·Product code LFL·November 10, 2024
NEXUS® ULTRASONIC SURGICAL ASPIRATOR SYSTEM
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·December 6, 2023
NEXUS® BONESCALPEL® 25MM BLUNT BLADE AND IRRIGATION TUBING KIT
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·February 27, 2025
NEXUS® BONESCALPEL® 25MM, BLUNT BLADE + IRRIGATION TUBING KIT
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·November 13, 2024
NEXUS® BONESCALPEL® 25MM, BLUNT BLADE + IRRIGATION TUBING KIT
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·November 13, 2024
PRESSON
FDA Adverse Event
Injury
·NEXUS SPINE, LLC·Product code MNI·September 19, 2024
PRESSON
FDA Adverse Event
Injury
·NEXUS SPINE, LLC·Product code MNI·March 2, 2023
PRESSON
FDA Adverse Event
Injury
·NEXUS SPINE, LLC·Product code MNI·September 11, 2023
TRANQUIL-L
FDA Adverse Event
Malfunction
·NEXUS SPINE, LLC·Product code MAX·September 11, 2023
PRESSON
FDA Adverse Event
Injury
·NEXUS SPINE, LLC·Product code MNI·July 15, 2022
PRESSON
FDA Adverse Event
Injury
·NEXUS SPINE, LLC·Product code MNI·January 18, 2024
NEXUS SPINE
FDA Adverse Event
Injury
·NEXUS SPINE, LLC·Product code NKB·April 1, 2026
NEXUS SPINE
FDA Adverse Event
Injury
·NEXUS SPINE, LLC·Product code OVD·March 11, 2026