12 results
·
21ms
·
Sources: EU EUDAMED, US FDA
ANTERIOR NECK CONTOUR COIL
FDA 510(k)
FDA Class 2
·Radiology
VuePoint
FDA UDI
Nuvasive, Inc.·00887517180391·VuePoint Screw, 3.5x12mm Fav Angle MA
Pyramesh® Implant System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00673978081038·MESH 905-512 PYRM 13 X 17 OVOID X 12MM
Pyramesh® Implant System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000856533·MESH 905-512 PYRM 13 X 17 OVOID X 12MM
Duo Lumbar Interbody Fusion Device
FDA UDI
SPINEOLOGY INC.·M7402905512·Duo, Non-Lordotic, 55 x 12mm
SIEMENS ELEMA MODELS 4020T AND 4021T ADAPTERS
FDA 510(k)
FDA Class 2
·Cardiovascular
L SOPHIA
FDA 510(k)
FDA Unclassified
·Unknown
BINAXNOW COVID-19 AG SELF TEST 4CT
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QYT·January 29, 2025
CS300 INTRA-AORTIC PUMP
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·May 28, 2014
LIPOSONIX
FDA Adverse Event
Injury
·SOLTA MEDICAL, INC.·Product code OHV·January 9, 2013
ARTICUL/EZE BALL 28 + 1.5 GR
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDI·November 19, 2010
AXIUM HELIX
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 8, 2020