67 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Zavation
FDA UDI
Zavation LLC·00842166183445·BOX CHISEL, 8mm
COR-VALV Atrial tissue retractor system
FDA UDI
Coroneo Inc·10817121000508·The COR-VALV Atrial retractor system is intende...
Marienfeld Superior
FDA UDI
Paul Marienfeld GmbH & Co. KG·04250317300010·
SAVANNAH
FDA UDI
SPINAL ELEMENTS·00840916151461·SAVANNAH®-T TAB BREAKER
OsteoMed
FDA UDI
OSTEOMED LLC·00845694001342·6mm Chin Plate
SAVANNAH-T
FDA UDI
SPINAL ELEMENTS·00840916149932·SAVANNAH®-T TAB BREAKER COLLAR
SAVANNAH-T
FDA UDI
SPINAL ELEMENTS·00840916149918·SAVANNAH®-T TAB BREAKER SHAFT
SAVANNAH-T
FDA UDI
SPINAL ELEMENTS·00840916149925·SAVANNAH®-T TAB BREAKER HANDLE
OsteoMed
FDA UDI
OSTEOMED LLC·00845694029728·6mm Chin Plate, Sterile
ELECSYS B-CROSSLAPS CALCHECK
FDA 510(k)
FDA Class 1
·Clinical Chemistry
CT PERFUSION 2
FDA 510(k)
FDA Class 2
·Radiology
OsteoMed
FDA UDI
OSTEOMED LLC·00845694063142·2.0 System 6mm Chin Plate Sterile Qty 2
GALASHAPE 3D
FDA Adverse Event
Injury
·TEPHA, INC.·Product code OOD·November 13, 2017
GALASHAPE 3D
FDA Adverse Event
Injury
·TEPHA, INC.·Product code OOD·November 13, 2017
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 28, 2025
Kit, Rna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·APTIMA HPV ASSAY
BATTERY OSCILLATOR II
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code GEY·January 28, 2014
Kit, Rna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·Aptima HPV Assay
Kit, Rna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·Aptima HPV Assay