26 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AURAGEN CORTICAL SURFACE ELECTRODES
FDA 510(k)
FDA Class 2
·Neurology
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X0822500·8mm H x 22mm W x 50mm L x 0 degrees XLIF
VK Couture
FDA UDI
Diversified Products, Inc.·00037741908265·
Clear Readers
FDA UDI
Diversified Products, Inc.·00842894127735·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16740822500·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X082250120·8mm H x 22mm W x 50mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L082250120·8mm H x 22mm W x 50mm L XLIF Trial 12 degree Lo...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X08225080·8mm H x 22mm W x 50mm L x 8 degrees XLIF
VK Couture
FDA UDI
Diversified Products, Inc.·00842894114995·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674082250060·
RAICHEM MULTI-ANALYTE CALIBRATOR
FDA 510(k)
FDA Class 2
·Clinical Chemistry
GEOFORM ANNULOPLASTY RING, MITRAL MODEL 4200
FDA 510(k)
FDA Class 2
·Cardiovascular
PAXGENE® BLOOD RNA TUBE
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code NTW·May 1, 2026
DXTEND GLENOSPHERE STD D42MM
FDA Adverse Event
Injury
·DEPUY FRANCE·Product code KWS·December 6, 2012
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·April 29, 2013
MINICAP TRANSFER SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·May 9, 2011
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIQ·July 24, 2008
UNSPECIFIED BD PAXGENE® BLOOD TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code PJE·June 13, 2025
PAXGENE® BLOOD RNA TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code NTW·March 23, 2026
PAXGENE® BLOOD RNA TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code NTW·March 31, 2026