22 results
·
41ms
·
Sources: EU EUDAMED, US FDA
PERIMETER INTERBODY FUSION DEVICE
FDA registration
Medtronic Engineering and Innovation Center (MEIC)·1 product·🇮🇳 India
PERIMETER INTERBODY FUSION DEVICE
FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·1 product·🇺🇸 United States
PERIMETER INTERBODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
RC Screw-retained Abutment
FDA UDI
BIO CONCEPT CO.,LTD·06947600381341·
PRECISION FORMS, INC.
FDA registration
PRECISION FORMS, INC.·1 product·🇺🇸 United States
Cholestech LDX Multianalyte Calibration Verification
FDA registration
Alere San Diego, Inc.·1 product·🇺🇸 United States
CONSTRUX PL/TL PEEK PARTIAL VBR SYSTEM
FDA registration
ORTHOFIX US LLC·1 product·🇺🇸 United States
Innomed, Inc.
FDA UDI
INNOMED, INC.·00840277100917·Cannestra Hip Length Gauge Set with Case
DISTAL RADIUS VOLAR RIM PLATE STANDARD AND NARROW
FDA registration
Changzhou Biomet Medical Devices Co., Ltd.·1 product·🇨🇳 China
Local Run Manager CF Clinical Seq 2 Micro Analysis Module
FDA registration
Illumina, Inc.·1 product·🇺🇸 United States
VR MEDICAL TECHNOLOGY CO., LTD.
FDA registration
VR MEDICAL TECHNOLOGY CO., LTD.·1 product·🇨🇳 China
Freedom Pedicle Screw System
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215027537·
BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS
FDA 510(k)
FDA Class 2
·Orthopedic
LIPID CONTROLS; MULTI- ANALYTE CONTROL; MULTI-ANALYTE CALIBRATION VERIFICATION MATERIALS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Spinal Vertebral Body Replacement Device
FDA classification
FDA Class 2
·Spinal Vertebral Body Replacement Device
Multi-Analyte Controls, All Kinds (Assayed)
FDA classification
FDA Class 1
·Multi-Analyte Controls, All Kinds (Assayed)
Patella Trial <41> mm SFP (264-1-10041)
FDA registration
Straits Orthopaedics (MFG) Sdn Bhd·1 product·🇲🇾 Malaysia
Patella Trial <41> mm SFP (264-1-10041)
FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia
Patella Trial <41> mm SFP (264-1-10041)
FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia