10 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SculpSure
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Oticon
FDA UDI
Oticon A/S·05707131282156·NERA2 PRO TI, BTE 13 WL 85 CNB
Scorpio
FDA UDI
Howmedica Osteonics Corp.·07613154020270·Posterior Stabilized Tibial Insert
SURE-POINT MIDLINE STEPPING AND STABILIZATION SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
OSSEOTITE II MODEL XIFOSSXXX
FDA 510(k)
FDA Class 2
·Dental
MONTERIS MEDICAL NEUROBLATE SYSTEM
FDA Adverse Event
Malfunction
·MONTERIS MEDICAL CORPORATION·Product code GEX·April 22, 2015
TALENT AAA
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·June 6, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 6, 2011
GE OEC 9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008
SYRINGE 1ML S/T U100 25G 1IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·April 14, 2021