10 results
·
26ms
·
Sources: EU EUDAMED, US FDA
CUSA SYSTEM 200C,T,M,H ULTRASONIC ASPIRATOR
FDA 510(k)
FDA Unclassified
·Unknown
InFix Anterior Lumbar Device
FDA UDI
Highridge Medical, LLC·00887868291388·Implant Base Tray
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756600996·EPIDURAL TRAY
LONG NAIL KIT R2.0, TI, LEFT GAMMA3 ?11X400MM X 13
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·December 4, 2012
RECOMB ECG PREAMPLIFIER/206 069 03
FDA 510(k)
FDA Class 2
·Cardiovascular
SLIP JOINT PLIERS
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·January 3, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP·Product code LZG·November 6, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·January 22, 2014
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021