54 results
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41ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Arthrosurface WristMotion Total Wrist Arthroplasty System
FDA 510(k)
FDA Class 2
·Orthopedic
SECURLINE UMBILICAL CORD CLAMP #3505 STERILE #3515 NON-STERILE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CHROMOSTREAK
FDA 510(k)
FDA Class 1
·Microbiology
UNK MAMMARY IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FWM·July 10, 2025
PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code NEW·April 22, 2018
PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code NEW·April 22, 2018
PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code NEW·April 22, 2018
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·April 22, 2018
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·April 22, 2018
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·April 22, 2018
BD VACUTAINER® MULTIPLE SAMPLE LUER ADAPTER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·March 21, 2019
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 29, 2025
EASY CORE BIOPSY DEVICE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FCG·November 5, 2009
EASY CORE BIOPSY DEVICE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FCG·November 5, 2009
EASY CORE BIOPSY DEVICE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FCG·November 5, 2009
EASY CORE BIOPSY DEVICE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FCG·November 5, 2009
EASY CORE BIOPSY DEVICE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FCG·November 5, 2009
UNKNOWN OPTEASE VENA CAVA FILTER
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code DTK·October 7, 2012
UNKNOWN OPTEASE VENA CAVA FILTER
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code DTK·October 7, 2012
RX ACCULINK CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code NIM·October 8, 2007