7 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Drug Relief
FDA 510(k)
FDA Class 2
·Neurology
AIDI DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
FLASH OSTIAL SYSTEM OTW-7.0MMX17MMX135CM, FLASH OSTIAL SYSTEM OTW-7.0MMX17MMX80CM
FDA 510(k)
FDA Class 2
·Cardiovascular
ENDOVIVE? STANDARD PEG KIT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code KNT·October 15, 2014
LOCKSCR Ø3.5 SELF-TAP L26 TAN
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code KTT·June 17, 2013
CONTAK RENEWAL
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 24, 2011
REMSTAR AUTO A-FLEX
FDA Adverse Event
Injury
·RESPIRONICS, INC.·Product code BZD·May 6, 2022