19 results
·
43ms
·
Sources: EU EUDAMED, US FDA
Gaitway Implant System
FDA registration
WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States
GAITWAY IMPLANT SYSTEM, SURGICAL INSTRUMENT SET
FDA 510(k)
FDA Class 2
·Orthopedic
ArgenZ HT+ 95x18 B1
FDA UDI
ARGEN CORPORATION, THE·D818122738·Dental porcelain/ceramic restoration kit
Durango
FDA registration
DONSON MACHINE COMPANY·4 products·🇺🇸 United States
Highridge Medical, LLC
FDA registration
Highridge Medical, LLC·4 products·🇺🇸 United States
RMS CO.
FDA registration
RMS CO.·4 products·🇺🇸 United States
Olive Branch Distribution Center
FDA registration
Olive Branch Distribution Center·4 products·🇺🇸 United States
LANX FUSION SYSTEM
FDA registration
MICROPULSE INC·4 products·🇺🇸 United States
catheter, percutaneous; catheter, angioplasty, peripheral, transluminal AGILTRAC 35 Peripheral Dilatation Catheter
FDA registration
Sterigenics Radiation Technologies, LLC·1 product·🇺🇸 United States
Mendell
FDA registration
Mendell·4 products·🇺🇸 United States
V2F
FDA registration
Sterigenics US LLC·1 product·🇺🇸 United States
BD Veritor System for Rapid Detection of Group A Strep CLIA waived kit
FDA registration
BECTON, DICKINSON & CO.·1 product·🇺🇸 United States
BD Veritor System for Rapid Detection of Group A Strep CLIA waived kit
FDA registration
BD Rapid Diagnostics (Suzhou) Co. Ltd.·1 product·🇨🇳 China
FORUM Archive and Viewer
FDA registration
CARL ZEISS MEDITEC AG (JENA)·1 product·🇩🇪 Germany
LANX FUSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
AGILTRAC .035 PERIPHERAL DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Screw, Fixation, Bone
FDA classification
FDA Class 2
·Screw, Fixation, Bone
Intervertebral Fusion Device With Integrated Fixation, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Integrated Fixation, Lumbar
Catheter, Percutaneous
FDA classification
FDA Class 2
·Catheter, Percutaneous