9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
TRANSEAR BONE CONDUCTION HEARING AID
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
CT LUCIA
FDA UDI
CARL ZEISS MEDITEC PRODUCTION, LLC·00843045100744·3-piece, monofocal, hydrophobic, acrylic, intra...
AERONOX UNIVERSAL, MODEL P/N 360000, AERONOX BEDSIDE, MODEL P/N 360001, AERONOX TRANSPORT TRANSPORT, MODEL P/N 360002
FDA 510(k)
FDA Class 2
·Anesthesiology
AT HOME DRUG TEST, MODEL 9068 T
FDA 510(k)
FDA Unclassified
·Unknown
MAXIM TIBIAL BEARING 10X71/75MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·April 10, 2013
RIATA ST ACTIVE FIXATION LEAD
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008
KAPPA 900 VDD
FDA Adverse Event
Malfunction
·MEDTRONIC S.A.·Product code DXY·April 12, 2011
LOGIC CR TIB INSERT SLOPE+, SZ 5, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 11, 2024
Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.
FDA Enforcement
Class II
·Terminated·Belmont Instrument Corporation·October 24, 2012