71 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SafePath Suturing System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002015·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002022·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002039·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002084·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002060·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002046·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002053·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002091·MCK Onlay Tibial Insert
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002077·MCK Onlay Tibial Insert
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100943·JAFFE LID RETRACTOR SMALL
SMARTEST PERSONA BLOOD GLUCOSE TEST SYTEM MODEL: 6277
FDA 510(k)
FDA Class 2
·Clinical Chemistry
SHIMADZU MOBILE X-RAY SYSTEM MOBILEDART EVOLUTION
FDA 510(k)
FDA Class 2
·Radiology
Vasomedical-Biox™ 1807 ABP Monitor With Analysis S/W w/ Bluetooth
FDA UDI
VASOMEDICAL, INC.·00817980020061·Ambulatory Blood Pressure Recorder w/Bluetooth
KYPHX HV-R BONE CEMENT
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code NDN·May 29, 2019
GALAXY G3 MINI 1MM X 4CM
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code KRD·November 15, 2021
NEEDLE 16GA 1-1/2IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·August 18, 2021
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