39 results · 36ms · Sources: EU EUDAMED, US FDA

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CUROS PORT PROTECTOR

FDA 510(k)
FDA Class 2 ·General Hospital

3D SCANNER, MODEL 1230

FDA 510(k)
FDA Class 2 ·Radiology

FHC MICROTARGETING DRIVE SYSTEM

FDA 510(k)
FDA Class 2 ·Neurology

CD SPINAL FIXATION SYSTEM

FDA Adverse Event
Injury ·SOFAMOR DANEK EUROPE·Product code KWP·May 19, 1999

LIPOSORBER LA-15

FDA Adverse Event
Other ·KANEKA CORP.·Product code MMY·December 23, 1997

GORE-TEX® CARDIOVASCULAR PATCH

FDA Adverse Event
Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DXZ·March 17, 2025

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·October 29, 2015

DRIVE

FDA Adverse Event
Injury ·A & I INDUSTRIES LTD·Product code ITJ·September 8, 2023

SILASTIC II

FDA Adverse Event
Malfunction ·DOW CORNING WRIGHT·Product code FTR·July 22, 1992

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·June 11, 2014

ACCU-CHEK ® PERFORMA TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 14, 2013

VERSASTEP PLUS 12MM CANN/DILT W/RADEXPSL

FDA Adverse Event
Malfunction ·PONCE - USS·Product code GCJ·August 12, 2008

OXFORD UNICOMPARTMENTAL KNEE PHASE 3 LEFT MEDIAL TIB TRAY STD SIZE E

FDA Adverse Event
Injury ·BIOMET UK LTD·Product code NRA·June 2, 2011

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·May 25, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·May 25, 2018

VENTILARM

FDA Adverse Event
Death ·VENTRONICS·Product code CBK·December 3, 1992

CADD-PCA

FDA Adverse Event
Malfunction ·PHARMACIA DELTEC·Product code MEA·October 8, 1992

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 22, 2017

CD HORIZON® SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code NKB·May 6, 2022

CD HORIZON® SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code NKB·May 6, 2022