7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RICHARDS TOTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
FLOW-I ANESTHESIA SYSTEM C20, C30 & C40
FDA 510(k)
FDA Class 2
·Anesthesiology
hekaDrill
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
WAGNER SL REVISION®, SCREW FOR TRIAL STEM, L 265
FDA Adverse Event
Injury
·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code JDI·May 4, 2022
FLOGARD
FDA Adverse Event
Malfunction
·SHARP CORPORATION OSAKA JAPAN·Product code FRN·January 29, 2013
STELIX II
FDA Adverse Event
Injury
·SORIN BIOMEDICA CRM S.R.L.·Product code DTB·December 21, 2010
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 15, 2014