8 results
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29ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DURALASTIC SILICONE TUBING
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
THE STACHROM HEPARIN ASSAY KIT
FDA 510(k)
FDA Class 2
·Hematology
CODMAN DISPOSABLE SCALP CLIP APPLIER
FDA 510(k)
FDA Class 2
·Neurology
NI
FDA Adverse Event
Malfunction
·VANTIVE US HEALTHCARE LLC·Product code KDI·October 23, 2025
LC PCA NEW 802.11 AB
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code MEA·June 12, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·February 11, 2013
LIGAMAX-5MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·January 10, 2011
SMALL SUPERIOR AUGMENT GLENOID PLATE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWS·February 22, 2024