75 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AOC BONE WAX, OSTENE, OSTEOTENE, ORTHOSEAL, OSTEOSEAL, CERETENE, MODEL BW-12
FDA 510(k)
FDA Unclassified
·Unknown
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306810824·Walden-Marshall breast dissection scissors with...
Tiche PTA Balloon Dilatation Catheter
FDA UDI
BrosMed Medical Co.,Ltd.·06958481475142·
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·January 28, 2022
Mariner Outrigger
FDA UDI
Seaspine Orthopedics Corporation·10889981173111·L Con, Side-Loading, R, 8mm, 440mm
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·January 28, 2022
Logical 20° Hooded Liner
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215095253·
HARDYDISK CEFTRIAXONE 30MCG
FDA 510(k)
FDA Class 2
·Microbiology
FREELITE LAMBDA FREE KIT
FDA 510(k)
FDA Class 2
·Immunology
Widex
FDA UDI
Widex A/S·05706069687064·Widex EVOKE E-IM (Dark brown ) 440, Right
Widex
FDA UDI
Widex A/S·05706069687057·Widex EVOKE E-IM (Clay brown ) 440, Right
Widex
FDA UDI
Widex A/S·05706069687040·Widex EVOKE E-IM (Light beige ) 440, Right
PRIMORIS HIP STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 5, 2016
PRIMORIS FEMORAL STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·October 3, 2017
PRIMORIS NECK PROSTH BM SZ 26
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 4, 2016
PRIMORIS HIP STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 5, 2016
PRMRS NCK STEM TI BM SZ 24 RSA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·June 23, 2016
MADIGAN ARMY TACOMA WA 1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DWE·December 7, 2009
TAPERLOC LAT COCR 10MM T1
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code JDI·March 20, 2026
TPRLOC COCR CMTD STEM T1 7.5MM
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code JDI·March 20, 2026