36 results
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50ms
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Sources: EU EUDAMED, US FDA
AR-8860DS Implant System, PARS Suture
FDA registration
R.K. Manufacturing·1 product·🇺🇸 United States
Arthrex Australia Pty Ltd.
FDA registration
Arthrex Australia Pty Ltd.·1 product·🇦🇺 Australia
ARTHREX, INC.
FDA registration
ARTHREX, INC.·1 product·🇺🇸 United States
Dorado TLIF Intervertebral Body Cage System/ Vega Span Spinous Process Plate/ Arena-L ALIFT Lumbar IBF System/ DORADO E-
FDA registration
Millstone Medical Outsourcing LLC·1 product·🇺🇸 United States
FlexiGRAFT GraftLink
FDA registration
LifeNet Health·1 product·🇺🇸 United States
STERILIZATION SERVICES OF GEORGIA, INC.
FDA registration
STERILIZATION SERVICES OF GEORGIA, INC.·1 product·🇺🇸 United States
INTERNATIONAL STERILIZATION LABORATORY, LLC
FDA registration
INTERNATIONAL STERILIZATION LABORATORY, LLC·1 product·🇺🇸 United States
Arthrex Logistic Center
FDA registration
Arthrex Logistic Center·1 product·🇺🇸 United States
FlexiGRAFT GraftLink
FDA registration
LIFENET HEALTH·1 product·🇺🇸 United States
Arthrex (Shanghai) Co., Ltd.
FDA registration
Arthrex (Shanghai) Co., Ltd.·1 product·🇨🇳 China
Arthrex Mexico, S.A. de C.V.
FDA registration
Arthrex Mexico, S.A. de C.V.·1 product·🇲🇽 Mexico
Ethyl Alcohol Enzyme Assay 25 mL Kit
FDA registration
Alere San Diego Inc.·1 product·🇺🇸 United States
SPINEFRONTIER LUMBAR IBF SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ARTHREX SUTURE GRAFTING KIT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Suture, Nonabsorbable, Synthetic, Polyethylene
FDA classification
FDA Class 2
·Suture, Nonabsorbable, Synthetic, Polyethylene
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar