7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MOSAIC DEVICES
FDA 510(k)
FDA Class 2
·Orthopedic
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704294217·
MB 103 MILLENNIUM BLADES
FDA 510(k)
FDA Class 1
·Ophthalmic
PREFERENCE TREATMENT SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
10NM TORQUE LIMITING RATCHET HANDLE-6MM HXC
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code LXH·April 22, 2013
CONMED SYSTEM 2450
FDA Adverse Event
Injury
·CONMED ELECTROSURGERY·Product code GEI·April 21, 2011
K-WIRE COCR, RECON 73.2X400 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·July 8, 2008