67 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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IMMAGE IMMUNOCHEMISTRY SYSTEM LIPOPROTEIN(A) LPAX REAGENT, ARRAY SYSTEM LIPOPROTEIN(A) LPA REAGENT, LIPOPROTEIN(A) CALIB
FDA 510(k)
FDA Class 2
·Immunology
Advance Dental Products
FDA UDI
The Atlanta Dental Supply Company·10850455007218·Advance Temporary Crown & Bridge Material A1 Ca...
Denar Slidematic Facebow
FDA UDI
WHIP-MIX CORPORATION·D04020001211·A facebow is a device intended for use in a den...
e-vive NMES System
FDA UDI
Motive Health, Inc.·00854691008124·e-vive NMES System; Extra Small, Right
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167700001210·
CURE 2.0 ACP
FDA UDI
SpineArt SA·07640375230867·CERVICAL 1 LEVEL TEMPLATE L21
CURE 2.0 ACP
FDA UDI
SpineArt SA·07640375232250·ANTERIOR CERVICAL PLATE, 1 LEVEL L21
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167S1700001210·
RX VIATRAC 14 PERIPHERAL DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
AESCULAP BONE WAX
FDA 510(k)
FDA Unclassified
·Unknown
EZ-28 DELIVERY SYSTEM
FDA Adverse Event
Injury
·BAUSCH & LOMB·Product code MSS·December 17, 2010
AZURION
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·January 9, 2025
VIS PÉDICULAIRE POLYAXIALE Ø5,5 LG50
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code NKB·April 28, 2016
VIS PÉDICULAIRE POLYAXIALE Ø5,5 LG40
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code NKB·April 28, 2016
NEURON DELIVERY CATHETER 070
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DQY·January 13, 2011
PROCLAIM 7 ELITE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 16, 2018
SWIFT-LOCK ANCHOR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·January 16, 2018
SWIFT-LOCK ANCHOR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·January 16, 2018
OCTRODE LEAD KIT, 60CM LENGTH
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code GZB·January 16, 2018
VASCUTRAK 2 PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·February 8, 2013