7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BinaxNOW COVID-19 Antigen Self Test
FDA 510(k)
FDA Class 2
·Microbiology
Valeo Spacer System and Valeo II Interbody Fusion Device System
FDA 510(k)
FDA Class 2
·Orthopedic
RADIOPAQUE BONE CEMENT
FDA 510(k)
FDA Class 2
·Orthopedic
VALEO / VALEO II
FDA Adverse Event
Malfunction
·SINTX TECHNOLOGIES (FORMERLY AMEDICA CORP)·Product code MAX·March 25, 2020
HARD TISSUE REPLACE(HTR(R))-PATIENT-MATCH IMPLANT
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code KKY·November 11, 2014
CLARION
FDA Adverse Event
Injury
·ADVANCED BIONICS, LLC·Product code MCM·August 30, 2011
OBTRYX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 23, 2013