10,000 results · 67ms · Sources: EU EUDAMED, US FDA

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CURO L5

FDA UDI
KPI HEALTHCARE, INC.·00860394001225·CURO L5 Cholesterol and Glucose measuring system

CURO L5 Total Cholesterol Strips

FDA UDI
KPI HEALTHCARE, INC.·00860394001256·Total Cholesterol Strips

Curo L5

FDA UDI
KPI HEALTHCARE, INC.·00850006113064·CURO L5 Glucose Strip

CURO B3

FDA UDI
KPI HEALTHCARE, INC.·00860394001232·CURO B3 Blood Pressure Monitor

CURO Glucose Strips

FDA UDI
KPI HEALTHCARE, INC.·00860394001294·CURO Glucose Strips for G6 and G6s

CURO G6s Smart Glucose Meter

FDA UDI
KPI HEALTHCARE, INC.·00860394001249·CURO G6s Smart Glucose Meter

CURO A1c

FDA UDI
KPI HEALTHCARE, INC.·00850006113026·CURO A1c Monthly Check Cartridge

CURO G6 Glucose Meter

FDA UDI
KPI HEALTHCARE, INC.·00860394001263·CURO G6 Glucose Meter

CURO A1c

FDA UDI
KPI HEALTHCARE, INC.·00850006113040·CURO A1c Daily Check Cartridge

Curo A1c Analyzer

FDA UDI
KPI HEALTHCARE, INC.·00860394001270·Curo A1c Analyzer

CURO A1c

FDA UDI
KPI HEALTHCARE, INC.·00850006113033·Curo A1c Test Cartridge

CARESTATION 750

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS (CHINA) CO., LTD (WUXI)·Product code BSZ·November 4, 2025

8100 ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·November 24, 2020

CARELINK PRO ONLINE

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code PHV·December 9, 2024

8100 ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·November 25, 2020

BD CATHENA 18GX1.25IN STRAIGHT BC

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FOZ·June 4, 2024

OMNIPOD DASH, PDM, PERSONAL DIABETES MANAGER

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code LZG·December 5, 2023

BD PYXIS¿ MEDSTATION¿ ES

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·June 9, 2025

NxTAG Respiratory Pathogen Panel +SARS-CoV-2, REF: I056C0468

FDA Recall
Open, Classified ·Luminex Molecular Diagnostics Inc·Product code QLT·September 5, 2024

NxTAG Respiratory Pathogen Panel, REF: I051C0447

FDA Recall
Open, Classified ·Luminex Molecular Diagnostics Inc·Product code OCC·September 5, 2024