10 results
·
17ms
·
Sources: EU EUDAMED, US FDA
DIGITAL RADIATION DETECTOR
FDA 510(k)
FDA Class 1
·Radiology
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293272·
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690117902·MODULAR TIBIA PUNCH DART Size 1-2
ANKLE HINDFOOT NAILING SYSTEM
FDA UDI
ORTHOFIX SRL·18053340347365·ANKLE HINDFOOT REVISION NAIL TI L300MM D11MM ST...
Scanmate Flex
FDA 510(k)
FDA Class 2
·Radiology
ANTLIA I WOUND IRRIGATION SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LOGIC KNEE COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·December 4, 2025
XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIQ·April 24, 2014
TAPERLOC PC 15.0MM T1
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·October 4, 2012
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·July 27, 2010