8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SYNTHES MANDIBLE EXTERNAL FIXATOR
FDA 510(k)
FDA Class 2
·Dental
HEDROCEL VERTEBRAL BODY REPLACEMENT, MODEL XX-YYY-ZZZZ
FDA 510(k)
FDA Class 2
·Orthopedic
BACT/ALERT MB CULTURE BOTTLE
FDA 510(k)
FDA Class 1
·Microbiology
HEMICAP/UNICAP RESURFACING PROSTHESIS
FDA Adverse Event
Other
·ARTHROSURFACE, INC.·Product code HSD·December 7, 2012
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·March 3, 2025
CONSTELLATION VISION SYSTEM
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·April 8, 2013
QUICKSITE LV
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·May 27, 2008
TRIAGE CARDIAC PROFILER
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC·Product code NBC·April 4, 2011