8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
NASOSTAT
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
Archon
FDA UDI
Nuvasive, Inc.·00887517658890·Archon Screw, Ø4.5x15mm Self Drill Vari
AUDI-SIL EARMOLD MATERIAL
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
OLYMPUS CEA - CARCINOEMBRYONIC ANTIGEN
FDA 510(k)
FDA Class 2
·Immunology
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·April 30, 2014
FENESTRATED BIPOLAR FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·October 10, 2012
VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code MAF·August 3, 2010
PROPONENT DR SL (Model L201)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025