8 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Diode Laser Therapy System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SUPERVAN 1.5T MAGNETIC RESONANCE IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
NASAL-AIR CRITICAL CARE
FDA 510(k)
FDA Class 2
·Anesthesiology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 21, 2025
IMPLANT, ENDOSSEOUS, ROOT-FORM
FDA Adverse Event
Injury
·J DENTAL CARE SRL·Product code DZE·August 28, 2025
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL MANUFACTURING CORPORATION·Product code MVK·October 17, 2014
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·September 1, 2011
PLV-100
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·July 15, 2013