24 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PreludeSYNC DISTAL Radial Compression System
FDA 510(k)
FDA Class 2
·Cardiovascular
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001636·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001087·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001063·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001629·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001605·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001612·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001643·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001650·MCK Inlay Tibial Component
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486001070·MCK Inlay Tibial Component
SignaLoc Screw
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215116743·
OLYMPUS EMPOWER H65
FDA Adverse Event
Malfunction
·QUANTA SYSTEM S.P.A.·Product code GEX·May 19, 2022
SRI LP GOWN
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DISPOSABLE CIRCULAR STAPLER, DISPOSABLE CIRCULAR STAPLER MODEL KYGW-25.5, KYGW-28.5
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD¿ SYRINGE WITH NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMF·October 30, 2018
PIPELINE
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·March 17, 2020
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·June 20, 2013
PED FLTR W/CLV
FDA Adverse Event
Malfunction
·HOSPIRA, LTD.·Product code FPA·May 5, 2011
3003135857-2008-00045
FDA Adverse Event
Malfunction
·Product code CBK·July 21, 2008
EXPRESSEW III AC+ GUN
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code LXH·February 1, 2022