21 results
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50ms
·
Sources: EU EUDAMED, US FDA
ProFound Detection (V4)
FDA registration
ICAD INC.·1 product·🇺🇸 United States
ProFound Detection (V4.0)
FDA 510(k)
FDA Class 2
·Radiology
Radiological Computer Assisted Detection/Diagnosis Software For Lesions Suspicious For Cancer
FDA classification
FDA Class 2
·Radiological Computer Assisted Detection/Diagnosis Software For Lesions Suspicious For Cancer
Ultra-Care Pen Needles 33G 5/32" 100 Ct
FDA UDI
ARISE MEDICAL LLC·00372217006077·Insulin Pen Needle
DIVERGENCE ANTERIOR CERVICAL FUSION SYSTEM
FDA registration
Sterigenics US, LLC·1 product·🇺🇸 United States
Freehand Inserter Sleeve
FDA registration
Engineered Medical Systems, LLC·2 products·🇺🇸 United States
STERIS ISOMEDIX PUERTO RICO, INC.
FDA registration
STERIS ISOMEDIX PUERTO RICO, INC.·2 products·🇺🇸 United States
DIVERGENCE(TM) Anterior Cervical Fusion System
FDA registration
WARSAW ORTHOPEDIC, INC.·2 products·🇺🇸 United States
DIVERGENCE(TM) Anterior Cervical Fusion System
FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·2 products·🇺🇸 United States
DIVERGENCE(TM) Anterior Cervical Fusion System
FDA registration
Medtronic Medical Costa Rica S.R.L.·2 products·🇨🇷 Costa Rica
DIVERGENCE(TM) Anterior Cervical Fusion System
FDA registration
MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO·2 products·🇺🇸 United States
DIVERGENCE(TM) Anterior Cervical Fusion System
FDA registration
MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·2 products·🇩🇪 Germany
DIVERGENCE(TM) Anterior Cervical Fusion System
FDA registration
Medtronic Engineering and Innovation Center (MEIC)·2 products·🇮🇳 India
DIVERGENCE(TM) Anterior Cervical Fusion System
FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·2 products·🇺🇸 United States
Pillar palatal
FDA registration
STERILIZATION SERVICES OF GEORGIA, INC.·1 product·🇺🇸 United States
cobas liat CT/NG nucleic acid test
FDA registration
ROCHE MOLECULAR SYSTEMS, INC.·3 products·🇺🇸 United States
VersaWrap
FDA registration
ALAFAIR BIOSCIENCES, INC.·1 product·🇺🇸 United States
DIVERGENCE MINI-PLATE ANTERIOR CERVICAL FUSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PILLAR PALATAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
Device, Anti-Snoring
FDA classification
FDA Class 2
·Device, Anti-Snoring