8 results
·
33ms
·
Sources: EU EUDAMED, US FDA
NONINVASIVE TEMPORARY PACEMAKER
FDA 510(k)
FDA Class 2
·Cardiovascular
Tranquil-C™
FDA UDI
NEXUS SPINE, L.L.C.·B6788222460·Cervical Rasp 12x14x12
MODIFICATION TO SYMPHONY GRAFT DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
MIST 360 SINGLE USE APPLICATOR KIT, MIST 360 SINGLE USE APPLICATOR KIT, CASE OF 12
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·March 2, 2023
INCLUSIVE TAPERED IMPLANT 5.2 X 13MM
FDA Adverse Event
Malfunction
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·May 20, 2014
UNKNOWN DEPUY AML CUP
FDA Adverse Event
Injury
·DEPUY WARSAW·Product code KWA·November 7, 2012
ZERO TIP STONE RETRIEVAL BASKET
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code FFL·August 12, 2010