25 results
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28ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SYNTHES TITANIUM MULTI-VECTOR DISTRACTOR
FDA 510(k)
FDA Class 2
·Dental
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040047453·Plugger Root Canal 8.5A
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890106900·Zirlux Titanium Esthetic Abutment Anterior comp...
Endo Carry-on Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964151729·Endo Carry-on Procedure Kit contains Intercept ...
PAUL HARTMANN AG
FDA registration
PAUL HARTMANN AG·9 products·🇩🇪 Germany
ASEPTIC TRANSFER KIT HOUSING
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL SA·Product code MOQ·June 8, 2021
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033188194·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033188156·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033188163·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033188187·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033188170·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033188149·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033188132·
PROTECTIV SAFETY BLOOD COLLECTION NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
3M RED DOT RADIOLUCENT MONITORING ELECTRODE WITH CONDUCTIVE ADHESIVE
FDA 510(k)
FDA Class 2
·Cardiovascular
YPSOPUMP INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·May 20, 2025
ACIST
FDA Adverse Event
Injury
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 14, 2013
ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY
FDA Adverse Event
Injury
·COOK, INC.·Product code MIH·February 25, 2011
RIATA PASSIVE FIXATION LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008