11 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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EMVERA DIOLUX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ArgenPMMA 95x30-B3
FDA UDI
ARGEN CORPORATION, THE·D818123257·Crown And Bridge, Temporary, Resin
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970584·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970591·
WAVEWRITER ALPHA 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 21, 2024
ENDOSCOPIC LASER DELIVERY SYSTEM-LASERTX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MLS, ZERONA-AD
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
NEW PROKIN·Product code FSA·May 21, 2013
UNKNOWN_RECONSTRUCTIVE_PRODUCT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWY·September 26, 2014
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 14, 2011
Quadra Assura, Sterile EO, Model #/ Part #: CD3265-40/100042335, 100059846; CD3265-40Q/100042336, 100059847; CD3267-40/100042956, 100043569, 100059961, 100078810; CD3267-40Q/100043132, 100043539, 100059917, 100059956, 100078904; CD3365-40C/100080435, 100080436; CD3365-40Q/100080426, 100080427; CD3367-40/100078813, 100079497, 100096097; CD3367-40C/100078597, 100079174, 100079450, 100079490, 100105524; CD3367-40Q/100078851, 100079212, 100079504, 100096098; CD3367-40QC/100078656, 100079193, 100079498, 100079524, 100105513, 100105514, 100138185, 100138213; CD3385-40C/100080778; CD3385-40QC/100080780, 100105489
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018