8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Picocare
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
IKONISCOPE ONCOFISH BLADDER TEST SYSTEM
FDA 510(k)
FDA Class 2
·Hematology
CERALAS E/ 1470NM FIBER-COUPLED DIODE LASER FAMILY; CREALAS HPD MULTIWAVELENGHT 980NM/ 1470NM FIBER-COUPLED DIODE LASER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 24, 2025
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·June 11, 2013
KYPHON INFLATABLE BONE TAMP
FDA Adverse Event
Injury
·MEDTRONIC SPINE LLC.·Product code HRX·July 14, 2011
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIQ·September 16, 2008
ALINITY S HIV AG/AB COMBO REAGENT KIT
FDA Adverse Event
Injury
·ABBOTT GMBH·Product code QHM·April 21, 2022