25 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PGS 5.5 MM CANNULATED PEDICLE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
CoRoent
FDA UDI
Nuvasive, Inc.·00887517637406·CoRoent Ant TLIF PEEK, 14x11x28mm 12°
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973851·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970904·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970898·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973141·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973318·
SCOUTPRO HEMOSTATIC VALVE
FDA 510(k)
FDA Class 2
·Cardiovascular
MODIFICATION TO TSRH SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TSRH® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·April 19, 2013
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC ORTHOPEDIC INC.·Product code KWP·December 4, 2009
HAHN TAPERED IMPLANT Ø4.03 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·July 9, 2024
HAHN TAPERED IMPLANT Ø4.3 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·April 5, 2024
HAHN TAPERED IMPLANT Ø4.3 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·November 21, 2025
HAHN TAPERED IMPLANT Ø4.3 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·April 23, 2024
HAHN TAPERED IMPLANT Ø4.3 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·August 7, 2024
HAHN TAPERED IMPLANT Ø4.3 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·July 10, 2024
HAHN TAPERED IMPLANT Ø4.3 X 8 MM
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT INC.·Product code DZE·April 15, 2025
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWP·December 4, 2009
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·May 29, 2013