674 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NuVasive Cohere Thoracolumbar Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741818600·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674181860060·
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074459820·ASSEMBLY 9181860 OF ALL-IN-1 FINAL
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1818600·18mm H x 18mm W x 60mm L x 0 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L181860120·18mm H x 18mm W x 60mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X181860120·18mm H x 18mm W x 60mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X18186080·18mm H x 18mm W x 60mm L x 8 degrees XLIF
NOVABONE PUTTY- BIOACTIVE SYNTHETIC BONE GRAFT
FDA 510(k)
FDA Class 2
·Orthopedic
ZIMMER SEGMENTAL SYSTEM VARIABLE STIFFNESS STEM EXTENSIONS AND INTERCALARY SEGMENTS
FDA 510(k)
FDA Class 2
·Orthopedic
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
UNKNOWN·Product code IKX·June 21, 2013
PROLENE POLYPROPYLENE SUTURE
FDA Adverse Event
Injury
·ETHICON·Product code GAW·July 28, 2011
GE OEC 9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 19, 2008
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 17, 2025
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 19, 2025
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code NJR·April 17, 2026
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 14, 2026
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026