21 results · 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