25 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Velmeni for Dentists (V4D)
FDA 510(k)
FDA Class 2
·Radiology
ADULT ENDOTRACHEAL CLOSED SUCTION SYSTEM 24 HOURS, SIZE 10F
FDA UDI
Intersurgical Incorporated·05030267115259·ADULT ENDOTRACHEAL CLOSED SUCTION SYSTEM 24 HOU...
MaXcess
FDA UDI
Nuvasive, Inc.·00887517195173·MaXcess 4 Crossbar, Anterior
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613327539806·STERNALPLATE, BOX
FIXED TARGETING INSERT
FDA UDI
Osteocentric Technologies, Inc.·00810189110311·FIXED TARGETING INSERT
ARKEO, Wedge Fixation System
FDA UDI
Auxano Medical LLC·00810199190051·ARKEO Wedge Impactor
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR32400031·SARA 3N spring with sleeve
Baby Gorilla/Gorilla Plating System
FDA UDI
Paragon 28, Inc.·00889795039965·LCF Joint Preparation Paddle
Aortic Stent
FDA Pre-Market Approval
FDA Class 3
·Minima Stent System
VERTEBRON SCP CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
COROENT SMALL INTERBODY SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Aortic Stent
FDA Pre-Market Approval
FDA Class 3
·Minima Stent System
Aortic Stent
FDA Pre-Market Approval
FDA Class 3
·Minima Stent System
Aortic Stent
FDA Pre-Market Approval
FDA Class 3
·Minima Stent System
Aortic Stent
FDA Pre-Market Approval
FDA Class 3
·Minima Stent System
Aortic Stent
FDA Pre-Market Approval
FDA Class 3
·Minima Stent System
Aortic Stent
FDA Pre-Market Approval
FDA Class 3
·Minima Stent System
SURVEIL DCB
FDA Adverse Event
Malfunction
·SURMODICS, INC.·Product code ONU·November 19, 2025
TOTAL ASR FEM IMPLANT SZ 55
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code JDI·November 19, 2008
ACCESS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FPA·September 8, 2011