56 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VITA YZ ST and VITA YZ XT
FDA 510(k)
FDA Class 2
·Dental
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002176·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002169·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002183·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486000868·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486000875·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002213·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002206·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486000851·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002190·MCK Onlay Tibial Insert
STATIONARY X-RAY SYSTEM (DETECTOR) MODEL: ALTAS
FDA 510(k)
FDA Class 2
·Radiology
BTI FILTRATION DEIONIZATION EXCHANGE TANK; BTI FILTRATION CARBON EXCHANGE TANK
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
KYPHX HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code NDN·May 29, 2019
KYPHON HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code NDN·April 29, 2019
KYPHON HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·June 6, 2019
KYPHON HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·September 20, 2019
KYPHON HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·July 15, 2019
KYPHON HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code NDN·March 25, 2020
KYPHX HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code NDN·October 11, 2019
KYPHON HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·October 6, 2019