8 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Altus Spine Interbody Fusion System
FDA 510(k)
FDA Class 2
·Orthopedic
OsteoMed
FDA UDI
OSTEOMED LLC·00842528127759·2.4 X 6mm Cannulated Headed Screw, T7
PASS ANTERIOR SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EXPANDABLE PEEK-OPTIMA IMPLANT
FDA 510(k)
FDA Class 2
·Orthopedic
SMART PERFUSION PACK: APEX MBR FMC/MID WEST REG LEXINGTON, KY
FDA Adverse Event
Injury
·Product code DTZ·September 11, 2007
GYNECARE TVT RETROPUBIC SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·June 21, 2013
VOYAGER NC CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·July 28, 2011
ACRYSOF TORIC
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./HUNTINGTON·Product code MJP·September 12, 2008