8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SURGICAL DRAPES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DINAMAP MODEL 855
FDA 510(k)
FDA Class 2
·Cardiovascular
PALPATION PROBE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
BONE ANCHOR SYSTEM FOR SOFT TISSUE SUPPORT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code MBI·April 27, 2012
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 1, 2024
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 1, 2013
SEQUOIA TI POLY SCREW ASSY 8.5MM X 45MM
FDA Adverse Event
Injury
·ZIMMER SPINE, INC.·Product code NKB·July 8, 2014
MINI-CAP, DISCONNECT W/PVP-1SOLUTION
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·January 26, 2011