674 results · 29ms · Sources: EU EUDAMED, 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