8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
MODIFIED BIOVAC:LFA LASER FUME EVACUATION SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GC Initial™
FDA UDI
Gc America Inc.·J0228745121·GC Initial™ Ti Powder Opaque OC3, 50g
Legacy™4 Healing Collar-Concave Profile
FDA UDI
IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307112280·
DART DAILY AIR REMOVAL TEST
FDA 510(k)
FDA Class 2
·General Hospital
SANDMILL RMS
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
LC PCA HOSPIRA MEDNE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code MEA·April 22, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 19, 2010
WHITESTAR SIGNATURE¿ SYSTEM
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS·Product code HQC·December 14, 2012