6 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DERMTOME BLADE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
PREVIEW ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Pulsaderm ACE-All Blue
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
X-STOP INTERSPINOUS SPACER SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NQO·February 14, 2013
LCS COMPLETE FEM POR L STD
FDA Adverse Event
Injury
·DEPUY (IRELAND)·Product code NJL·January 7, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014