660 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TRIDENT ALL POLY CUP
FDA 510(k)
FDA Class 2
·Orthopedic
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040047644·Curette Goldman Fox 21
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040008225·Zirlux 16+ B4 89x17x14
INTER FIX™ RP Threaded Fusion Device
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00673978957500·20X26 INTERFIXRP FUSION DEVICE
CovaWound™ Silicone 20x26
FDA UDI
Covalon Technologies Ltd·00825439016077·Self-Adherent Soft Silicone Foam Dressing with ...
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033368619·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033368640·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033368657·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033368633·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033368626·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00193033368664·
Intess C
FDA UDI
Kalitec Direct LLC·B07309K0100260·Assembly, Caddie, Implants, Hinged
EMBOGOLD MICROSPHERE
FDA 510(k)
FDA Class 2
·Neurology
CAPIOX ARTERIAL FILTER
FDA 510(k)
FDA Class 2
·Cardiovascular
SPINNING SPIROS® CLOSED MALE LUER, RED CAP
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·August 10, 2022
MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 13, 2026
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·January 22, 2026
DeRoyal CATARACT PACK, REF 89-10040.01
FDA Enforcement
Class II
·Ongoing·DeRoyal Industries Inc·December 21, 2022
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 14, 2007
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 20, 2013