9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STIEGMANN-GOFF ENDOSCOPIC LIGATOR
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
UNKNOWN VLOC PRODUCT
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·December 21, 2023
RADENT PROPHY PASTE
FDA 510(k)
FDA Class 1
·Dental
Geistlich Bio-Oss®
FDA 510(k)
FDA Class 2
·Dental
METHYL METHACRYLATE
FDA Adverse Event
Death
·HOWMEDICA, INC.·Product code LOD·August 14, 1995
CLEARVIEW UTERINE MANIPULATOR
FDA Adverse Event
Injury
·CLINICAL INNOVATIONS, LLC·Product code LKF·June 11, 2024
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·June 25, 2014
ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE SYSTEM
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NTE·December 29, 2010
ANCHORAGE STANDARD SCREW 3.5MM X 16MM STERILE
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS SELZACH·Product code LXH·December 12, 2012