185 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Renovis Tesera C/Tesera SC Anterior Cervical Fusion (ACF) System
FDA 510(k)
FDA Class 2
·Orthopedic
OsteoMed
FDA UDI
OSTEOMED LLC·00842528128855·2.0mm x 7mm Cannulated Lag Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694005463·165mm x 95mm Rigid Osteoform Mesh Plate
CARTO 3 EP NAVIGATION SYSTEM, VERSION 2.2
FDA 510(k)
FDA Class 2
·Cardiovascular
PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,
FDA 510(k)
FDA Class 2
·Anesthesiology
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818460·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818422·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818446·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818415·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818453·
Persona® Partial Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304818439·
SYNCHROMED EL
FDA Adverse Event
Injury
·RICE CREEK MANUFACTURING·Product code LKK·October 22, 2008
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 28, 2021
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·May 8, 2009
SYNCRHOMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·May 8, 2009
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 24, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 28, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·November 7, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 29, 2021