31 results
·
49ms
·
Sources: EU EUDAMED, US FDA
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010418·PedFuse Reset, SLD, 9.0mm x 35mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010449·PedFuse Reset, SLD, 9.0mm x 50mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010494·PedFuse Reset, SLD, 9.0mm x 75mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010470·PedFuse Reset, SLD, 9.0mm x 65mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010500·PedFuse Reset, SLD, 9.0mm x 80mm
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361010432·PedFuse Reset, SLD, 9.0mm x 45mm
MODIFIED STRAIGHT FIRE LASER FIBER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EXTRICARE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Negative Pressure Wound Therapy Powered Suction Pump
FDA classification
FDA Class 2
·Negative Pressure Wound Therapy Powered Suction Pump
Powered Laser Surgical Instrument
FDA classification
FDA Class 2
·Powered Laser Surgical Instrument