71 results · 27ms · Sources: EU EUDAMED, 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