16 results
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45ms
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Sources: EU EUDAMED, US FDA
SHURFIT ACIF SYSTEM
FDA registration
Precision Spine, Inc.·1 product·🇺🇸 United States
NuTech Spine Interbody Cervical
FDA registration
NUTECH SPINE, INC.·1 product·🇺🇸 United States
QUALITY TECH SERVICES, LLC
FDA registration
QUALITY TECH SERVICES, LLC·1 product·🇺🇸 United States
Isomedix Operations, Inc.
FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States
SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
ZHERMACK S.P.A.
FDA registration
ZHERMACK S.P.A.·1 product·🇮🇹 Italy
Bipro Model SDS-CB200
FDA registration
MEDICAL SOLUTIONS INTERNATIONAL, INC.·1 product·🇺🇸 United States
Chromaclone Ortho 5 Day Stability
FDA registration
Ultradent Products Inc. / OraTech LLC·1 product·🇺🇸 United States
Primado Surgical System
FDA registration
NAKANISHI INC.·1 product·🇯🇵 Japan
Xpert HemosIL FII & FV
FDA registration
Cepheid·3 products·🇺🇸 United States
Primado Surgical System
FDA registration
NSK AMERICA CORP.·1 product·🇺🇸 United States
MODIFICATION TO ALPHA DX SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Z2 BALLOON GUIDED PACING & PRESSURE MONITORING CATHETER, MODEL Z2-7-02-1-10-0
FDA 510(k)
FDA Class 2
·Cardiovascular
Intervertebral Fusion Device With Bone Graft, Cervical
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Cervical
Fluorometric Method, Cpk Or Isoenzymes
FDA classification
FDA Class 2
·Fluorometric Method, Cpk Or Isoenzymes
Catheter, Flow Directed
FDA classification
FDA Class 2
·Catheter, Flow Directed