56 results · 21ms · Sources: EU EUDAMED, 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