204 results
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37ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EPIQ Diagnostic Ultrasound System Series, Affiniti Diagnostic Ultrasound System Series, CX50 Diagnostic Ultrasound System, Sparq Diagnostic Ultrasound System, Lumify Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
OsteoMed
FDA UDI
OSTEOMED LLC·00845694032223·2.0mm/2.4mm Threaded Tak
Zavation
FDA UDI
Zavation LLC·00842166132085·Ti3Z CIF 12mmx14mmx12mm -10 deg
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193113333·HA PEEK EVOS Straight, ,12mmx8mmx 26mm , FLAT ...
A-CIFT® SoloFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361021490·A-CIFT SoloFuse 4.2 Screw, Rigid, 12mm
NA
FDA UDI
Biedermann Motech GmbH & Co. KG·04250869683777·MOSS VRS Tower
OsteoMed
FDA UDI
OSTEOMED LLC·00845694073127·HPS 2.0mm/2.4mm Threaded Tak™ Sterile Qty 2
LAMINARIA 2MM/3MM/4MM/5MM/6MM/7MM/8MM/9MM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
DIGITAL INTEGRATION SYSTEM, DIS2000
FDA 510(k)
FDA Class 2
·Radiology
QUICK-CROSS SELECT SUPPORT CATHETER
FDA Adverse Event
Death
·SPECTRANETICS CORP.·Product code DQY·December 17, 2010
MAXIMO DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code LWS·February 14, 2011
ETHICON
FDA Adverse Event
Malfunction
·Product code GDW·March 22, 2010
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·January 6, 2011
INTRINSIC
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code LWS·June 16, 2011
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·January 7, 2011
CARDIOHELP SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTQ·November 26, 2014
CARDIOHELP SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTQ·November 26, 2014
CARDIOHELP SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTQ·November 26, 2014
MYNX VASCULAR CLOSURE DEVICE
FDA Adverse Event
Malfunction
·ACCESSCLOSURE, INC.·Product code MGB·April 2, 2010
BIOMED OXFORD TIBIA 2 RK
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code HRY·December 13, 2018