25 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD
FDA 510(k)
FDA Class 2
·Cardiovascular
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040013311·Zirlux 16+ D2 98.5X12
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033221792·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033221723·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033221747·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033221761·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033221778·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033221709·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033221754·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033221730·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033221785·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033221716·
OLYMPIC WARM-UP
FDA 510(k)
FDA Class 2
·Physical Medicine
UTERINE MANIPULATOR INJECTOR CANNULA, STERILE, MODEL R 57-450
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·January 13, 2025
NA
FDA UDI
Orthosoft Inc·00889024305458·
NA
FDA UDI
Orthosoft Inc·00889024305465·
INTELLIS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·April 30, 2026
UNK HARMONYCA LIDOCAINE
FDA Adverse Event
Injury
·PANAXIA LTD·Product code LMH·August 23, 2024
SINGLE LUMEN PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER SET
FDA Adverse Event
Injury
·COOK, INC.·Product code DQY·March 13, 2013