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

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DIXI Medical Microdeep Depth Electrode

FDA 510(k)
FDA Class 2 ·Neurology

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970362·

SPECIMEN RETRIEVAL SYSTEM

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

ORTHOPEDIATRICS BLADE PLATE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

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

ACCUDRAIN WITH ANTI-REFLUX VALVE

FDA Adverse Event
Malfunction ·INTEGRA NEUROSCIENCES PR·Product code JXG·June 11, 2018

ACCU-CHEK ® MOBILE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 14, 2014

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 14, 2013

PERFUSOR BASIC

FDA Adverse Event
Malfunction ·B. BRAUN MEDICAL, INC.·Product code FRN·June 30, 2011

I-STAT CHEM8+ CARTRIDGE (SEE H10 FOR EC8+)

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 7, 2017

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