18 results · 27ms · Sources: EU EUDAMED, US FDA

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CRE Pulmonary Balloon Dilatation Catheter

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·March 31, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·June 11, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·May 30, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·March 5, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·June 5, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·January 28, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·July 28, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·September 30, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·May 12, 2025

CRE PULMONARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KTI·January 10, 2025

BLAKE DRAIN UNKNOWN PRODUCT

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code GBX·April 7, 2021

POWERED EZ-IO PEDIATRIC BONE MARROW ASPIRATION SYSTEM

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

TEMPOCEM

FDA 510(k)
FDA Class 1 ·Dental

ALARIS PCA MODULE

FDA Adverse Event
Malfunction ·CAREFUSION CORP.·Product code FRN·May 22, 2013

ACCU-CHEK AVIVA TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 15, 2008

CENTURY BED

FDA Adverse Event
Malfunction ·HILL-ROM INC.·Product code FNL·June 22, 2011

VASERLIPO SYSTEM

FDA Adverse Event
Injury ·SOLTA MEDICAL, INC·Product code QPB·January 9, 2023