7 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ORTHOMET ACETABULAR ROOF REINFORCEMENT RING
FDA 510(k)
FDA Class 2
·Orthopedic
VIASPAN
FDA Adverse Event
Other
·FRESENIUS KABI AUSTRIA GMBH·Product code KDL·March 26, 2012
ABUSCREEN ONTRAK FOR THC
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ME20 TRACERITE CLEAR VENT TAPE, ME30 TRACERITE NON
FDA 510(k)
FDA Class 2
·Cardiovascular
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·February 5, 2013
STAPLE, IMPLANTABLE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 3, 2011
RELIANT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code DQY·July 18, 2014