15 results · 45ms · Sources: EU EUDAMED, US FDA

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VERTEBRAL BODY SET/SMALL- STERILE

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code KWQ·August 9, 2021

DRIVER SHAFT, T-15, LONG

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code LXH·September 13, 2018

TRUSTEEL

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·January 16, 2025

DRIVER SHAFT, T-15, LONG

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

DRIVER SHAFT, T-15, LONG

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

DRIVER SHAFT, T-15, MEDIUM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

DRIVER SHAFT, T-15, MEDIUM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

DRIVER SHAFT, T-15, MEDIUM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

3.0MM HEX DRIVER

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

DRIVER SHAFT, T-15, MEDIUM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

PERIPHERAL SCREW, NL, UNI REV, 4.5X42MM

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code KWS·June 5, 2019

HEART START XL

FDA Adverse Event
Death ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 7, 2013

GORE EXCLUDER AAA ENDOPROSTHESIS

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code MIH·February 18, 2011

STRATA 2 SHUNT ASSEMBLY, SMALL

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·February 18, 2008

DRIVER SHAFT, T-15, LONG

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code LXH·June 5, 2019