18 results
·
42ms
·
Sources: EU EUDAMED, US FDA
Intervertebral Body Fusion Device
FDA registration
MEDICAL DEVICE AND IMPLANTS LLC·1 product·🇺🇸 United States
nvt
FDA registration
NVISION BIOMEDICAL TECHNOLOGIES, INC·1 product·🇺🇸 United States
nva, nvp, nvt
FDA 510(k)
FDA Class 2
·Orthopedic
iO-Flex
FDA registration
SPINAL ELEMENTS, INC.·1 product·🇺🇸 United States
DARCO LOCKING BONE PLATE SYSTEM
FDA registration
SYMMETRY MEDICAL MANUFACTURING INC·1 product·🇺🇸 United States
DARCO LOCKING BONE PLATE SYSTEM
FDA registration
SYMMETRY MEDICAL MANUFACTURING INC·1 product·🇺🇸 United States
CrossCheck Plating System
FDA registration
WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States
DARCO LOCKING BONE PLATE SYSTEM
FDA registration
SYMMETRY MEDICAL MANUFACTURING INC.·1 product·🇺🇸 United States
CrossCheck Plating System
FDA registration
WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States
DEGANIA SILICONE, LTD.
FDA registration
DEGANIA SILICONE, LTD.·1 product·🇮🇱 Israel
Vienna System
FDA registration
SYNTHES GMBH·1 product·🇨🇭 Switzerland
JMS SINGAPORE PTE. LTD
FDA registration
JMS SINGAPORE PTE. LTD·2 products·🇸🇬 Singapore
PT JMS BATAM
FDA registration
PT JMS BATAM·2 products·🇮🇩 Indonesia
VANGUARD REPROCESSED NON-ELECTRIC BIOPSY FORCEPS
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
IO-FLEX CATHETER
FDA 510(k)
FDA Class 2
·Anesthesiology
Forceps, Biopsy, Non-Electric, Reprocessed
FDA classification
FDA Class 1
·Forceps, Biopsy, Non-Electric, Reprocessed
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Catheter, Conduction, Anesthetic
FDA classification
FDA Class 2
·Catheter, Conduction, Anesthetic