20 results
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42ms
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Sources: EU EUDAMED, US FDA
TigerShark M Interbody System
FDA registration
Choice Spine·1 product·🇺🇸 United States
Apex (Guangzhou) Tools & Orthopedics Company
FDA registration
Apex (Guangzhou) Tools & Orthopedics Company·1 product·🇨🇳 China
P070-6140 TLIF-Straight Bayonetted Cup Curette, #2
FDA registration
Straits Orthopaedics (MFG) Sdn Bhd·1 product·🇲🇾 Malaysia
P070-6140 TLIF-Straight Bayonetted Cup Curette, #2
FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia
P070-6140 TLIF-Straight Bayonetted Cup Curette, #2
FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia
ChoiceSpine TigerShark M, Modular Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
BD BBL™ Lysine Iron Agar Slants
FDA UDI
BECTON, DICKINSON AND COMPANY·30382902209530·BD BBL™ Lysine Iron Agar Slants
Pleur-evac Sahara® Plus Continuous Reinfusion Autotransfusion System
FDA registration
Teleflex Medical LLC·1 product·🇺🇸 United States
Pleur-evac Sahara® Plus Continuous Reinfusion Autotransfusion System
FDA registration
Teleflex Medical de Mexico, S. de R.L. de C.V.·1 product·🇲🇽 Mexico
MILLSTONE MEDICAL OUTSOURCING LLC.
FDA registration
MILLSTONE MEDICAL OUTSOURCING LLC.·3 products·🇺🇸 United States
Cohere
FDA registration
GLOBUS MEDICAL, INC.·3 products·🇺🇸 United States
MACKAY MANUFACTURING, INC.
FDA registration
MACKAY MANUFACTURING, INC.·3 products·🇺🇸 United States
NuVasive® Cohere® Thoracolumbar Interbody System
FDA registration
NUVASIVE, INC.·3 products·🇺🇸 United States
Pleur-evac Sahara® Plus Continuous Reinfusion Autotransfusion System
FDA registration
Teleflex LLC (NADC)·1 product·🇺🇸 United States
Cohere
FDA registration
NuVasive Manufacturing, LLC·3 products·🇺🇸 United States
DK2620JI FUJIFILM Diathermic Slitter (FlushKnife)
FDA registration
FUJIFILM CORPORATION·1 product·🇯🇵 Japan
NuVasive® Cohere® Thoracolumbar Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
PLEUR-EVAC SAHARA PLUS CONTINOUS REINFUSION AUTOTRANSFUSION SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Apparatus, Autotransfusion
FDA classification
FDA Class 2
·Apparatus, Autotransfusion