39 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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