32 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INCLUSIVE TAPERED IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
INCLUSIVE TAPERED IMPLANT
FDA Adverse Event
Malfunction
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·May 17, 2018
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813865·GENUMEDI PRO SILVER SIZE VI
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321214060·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311214060·
INTRACAPULAR MANIPULATING WAND
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896013124·INTRACAPULAR MANIPULATING WAND ANGLED TIP TITANIUM
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515016910·Olsen-Hegar N.H., 6 1/2"
TAPERLOC®
FDA UDI
Biomet Orthopedics, LLC·00880304430747·
BEVER REINFORCED ENDOTRACHEAL TUBE WITH CUFF (ORAL/NASAL), BEVER REINFORCED ENDOTRACHEAL TUBE WITHOUT CUFF (ORAL/NASAL)
FDA 510(k)
FDA Class 2
·Anesthesiology
ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001
FDA 510(k)
FDA Class 2
·Cardiovascular
BD PHOENIX¿ PID
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LQL·September 2, 2025
Anterior Cervical IBFD EX
FDA UDI
KEOS·B084AC4121406070·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072004111·MINI-VAC
Anterior Cervical IBFD
FDA UDI
KEOS·B084AC1121406040·
Anterior Cervical IBFD
FDA UDI
KEOS·B084AC2121406070·
Anterior Cervical IBFD
FDA UDI
KEOS·B084AC1121406070·
Anterior Cervical IBFD
FDA UDI
KEOS·B084AC1121406000·
BD PHOENIX¿ PID
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LQL·September 26, 2024
BD PHOENIX¿ PID
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LQL·September 26, 2024
Ascendant
FDA UDI
Choice Spine, LP·10885862260963·