18 results
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40ms
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Sources: EU EUDAMED, US FDA
Ti/HA Peg & Sleeve System
FDA registration
FCI SAS·1 product·🇫🇷 France
Ti/HA Peg & Sleeve System
FDA registration
FCI FRANCE CHIRURGIE INSTRUMENTATION·1 product·🇫🇷 France
Ti/HA Peg & Sleeve System
FDA registration
FCI SUD·1 product·🇲🇺 Mauritius
TITANIUM PEG SYSTEM
FDA 510(k)
FDA Class 2
·Ophthalmic
Ocular Peg
FDA classification
FDA Class 2
·Ocular Peg
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074088457·INSTRUMENT 2980822 8X22MM DSTRCTR TRIAL
Spark Violet™ 423 anti-human CD4
FDA UDI
BIOLEGEND, INC.·00810034702913·URL: https://www.biolegend.com/en-us/products/s...
Millstone Medical Outsourcing LLC
FDA registration
Millstone Medical Outsourcing LLC·1 product·🇺🇸 United States
Sterigenics US LLC
FDA registration
Sterigenics US LLC·2 products·🇺🇸 United States
Vu aPOD Intervertebral Body Fusion
FDA registration
SEASPINE ORTHOPEDICS CORPORATION·1 product·🇺🇸 United States
VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System
FDA registration
Wenzel Spine·2 products·🇺🇸 United States
Varilift
FDA registration
MAINSTREAM MEDICAL DEVICES·2 products·🇺🇸 United States
Isomedix Operations, Inc.
FDA registration
Isomedix Operations, Inc.·2 products·🇺🇸 United States
VariLift-C Interbody Fusion System
FDA registration
Safe Medical·2 products·🇫🇷 France
VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System
FDA 510(k)
FDA Class 2
·Orthopedic
VU APOD INTERVERTABRAL BODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
Intervertebral Fusion Device With Integrated Fixation, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Integrated Fixation, Lumbar
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar