97 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DMP ETCHING GEL
FDA 510(k)
FDA Class 2
·Dental
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814688·GENUMEDI SILVER SIZE V
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1022550·10mm H x 22mm W x 55mm L x 0 degrees XLIF
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741022550·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X10225580·10mm H x 22mm W x 55mm L x 8 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L102255120·10mm H x 22mm W x 55mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X102255120·10mm H x 22mm W x 55mm L x 12 degrees XLIF
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674102255060·
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523129911·Reduction Screw Implant Caddy for 5.5mm Rod
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973677·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970034·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973004·
MEDTRONIC SOFAMOR DANEK CEMENT RESTRICTOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE (MADGIC)
FDA 510(k)
FDA Class 2
·Anesthesiology
APPLIANCE, FIXATION, SPINAL INTERLAMINAL
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWP·December 7, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 27, 2020
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 27, 2020
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 20, 2015
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 27, 2020
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NKB·May 1, 2014