7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VERITON CT whole body SPECT/CT system
FDA 510(k)
FDA Class 2
·Radiology
ACCELAWAVE SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SEQURE SNARE SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
ACCU-CHEK SPIRIT ADAPTER
FDA Adverse Event
Injury
·DISETRONIC MEDICAL SYSTEMS, INC.·Product code LZG·December 21, 2007
ULTRACISION HARMONIC SCALPEL HANDPIECE
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·October 3, 2008
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 14, 2013
UNKNOWN PCA R FEMORAL COMPONENT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·July 19, 2011