28 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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STIMULAN KIT, STIMULAN RAPID CURE
FDA 510(k)
FDA Class 2
·Orthopedic
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1418300·14mm H x 18mm W x 30mm L x 0 degrees XLIF
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741418300·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L141830120·14mm H x 18mm W x 30mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X141830120·14mm H x 18mm W x 30mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X14183080·14mm H x 18mm W x 30mm L x 8 degrees XLIF
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981246860·Interbody, 43mm x 30mm X 18mm, 30 Deg
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981266110·Trial, 43mm x 30mm x 18mm, 30 Deg
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321418300·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311418300·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674141830060·
Vu a-POD Prime NanoMetalene
FDA UDI
Seaspine Orthopedics Corporation·10889981126827·Prime NM Implant, 31x24mm x 18mm, 30 Deg
MAGELLAN RATIO DISPENSER KIT
FDA 510(k)
FDA Class 2
·General Hospital
ZMACHINE, MODEL DT-100
FDA 510(k)
FDA Class 2
·Neurology
AP409 -PRIMARY INFUSION SET WITH VENTED/NON-VENTED DRIP CHAMBER
FDA Adverse Event
Malfunction
·EITAN MEDICAL LTD.·Product code FPA·December 18, 2025
AP205 - INFUSION SET WITH NON-VENTED SPIKE, 1.2UM FILTER AND NEEDLE Y-SITE
FDA Adverse Event
Malfunction
·EITAN MEDICAL LTD.·Product code FPA·June 5, 2024
AP210 - MICROBORE WITH NON-VENTED SPIKE AND 1.2UM FILTER
FDA Adverse Event
Malfunction
·EITAN MEDICAL LTD.·Product code FPA·June 6, 2024
AP210 - MICROBORE WITH NON-VENTED SPIKE AND 1.2UM FILTER
FDA Adverse Event
Malfunction
·EITAN MEDICAL LTD.·Product code FPA·June 17, 2024
BD INSYTE AUTOG BC
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 21, 2025
AP403 - MICROBORE INFUSION SET WITH VENTED/NON-VENTED SPIKE
FDA Adverse Event
Malfunction
·EITAN MEDICAL LTD.·Product code FPA·March 31, 2026