41 results
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28ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ACUMATCH A-SERIES CORUNDUM ACETABULAR COMPONENT AND ACUMATCH A-SERIES CORUNDUM ACETABULAR COMPONENT WITH HYDROXYAPATITE
FDA 510(k)
FDA Class 2
·Orthopedic
SR Facebow
FDA UDI
ORMCO CORPORATION·00889989023336·Facebow MINI-VEC SZ 2 .044 DIA
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·January 15, 2025
CURE ACP
FDA UDI
SpineArt SA·07640270064598·ANTERIOR CERVICAL PLATE, 2 LEVELS L42
Electrode
FDA UDI
I.C. MEDICAL, INC.·00817688020912·
CarboJet® CO2 Bone Lavage System
FDA UDI
Kinamed, Inc.·00818720011783·VacuJet® Suction Tube
CURE IVIEW
FDA UDI
MEDITECH SPINE, LLC·B167900002420·
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167700002420·
CarboJet® CO2 Bone Lavage System
FDA UDI
Kinamed, Inc.·00898142001500·Femoral Suction Tube
ELECSYS B-CROSSLAPS CALCHECK
FDA 510(k)
FDA Class 1
·Clinical Chemistry
MIDAS TOUCH LATEX EXAMINATION GLOVES-POWDER FREE
FDA 510(k)
FDA Class 1
·General Hospital
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167S1700002420·
CURE IVIEW
FDA UDI
MEDITECH SPINE, LLC·B167S1900002420·
CURE 2.0 ACP
FDA UDI
SpineArt SA·07640375231109·CERVICAL 2 LEVEL TEMPLATE L42
CURE 2.0 ACP
FDA UDI
SpineArt SA·07640375232700·ANTERIOR CERVICAL PLATE, 2 LEVELS L42
CURE 2.0™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167S11000002420·
OPEL-L
FDA UDI
SpineArt SA·07640332477298·OPEL-L IVIEW PLATE ASSEMBLY, L42
CURE ACP
FDA UDI
SpineArt SA·07640270064802·ANTERIOR CERVICAL PLATE, 2 LEVELS L42
CURE 2.0™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167T1000002420·
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·September 8, 2024