2,797 results · 30ms · Sources: EU EUDAMED, US FDA

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AERO AL INSERTER - DISTRACTOR

FDA Adverse Event
Injury ·STRYKER SPINE-FRANCE·Product code LXH·March 24, 2015

OP-1

FDA Adverse Event
STRYKER BIOTECH·Product code MPY·February 22, 2008

UNK - CAGE/SPACERS: CONTACT FUSION

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MNH·May 6, 2021

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·August 5, 2015

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·August 5, 2015

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 5, 2015

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 5, 2015

CALSTRUX

FDA Adverse Event
Product code MPY·February 22, 2008

MEDLINE INDUSTRIES, INC.

FDA Adverse Event
Malfunction ·MEDLINE INDUSTRIES, INC.·Product code FDE·September 16, 2024

UNK - CAGE/SPACERS: CONTACT FUSION

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MNH·May 6, 2021

CD HORIZON® SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 20, 2024

CD HORIZON® SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 20, 2024

GEN LAPAROSCOPY #536335-P-LF

FDA Adverse Event
Injury ·MEDLINE INDUSTRIES LP·Product code FDE·October 14, 2024

1030489-2017-00539

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code MQP·March 15, 2017

1030489-2017-00542

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code HWC·March 15, 2017

1030489-2017-00545

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code MAX·March 15, 2017

PROBE

FDA Adverse Event
MEDTRONIC SOFAMOR DANEK USA, INC·Product code HXB·February 3, 2015

XIA II HOOK FORCEPS

FDA Adverse Event
Malfunction ·STRYKER SPINE BORDEUX·Product code LXH·January 2, 2009

XIA BLOCKER

FDA Adverse Event
Injury ·STRYKER SPINE BORDEAUX·Product code KWP·December 13, 2005

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWP·July 16, 2008