8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
AMERLITE FERRITIN ASSAY, LAN.0800/1800/2800
FDA 510(k)
FDA Class 2
·Immunology
GC Initial™
FDA UDI
Gc America Inc.·J0228742031·GC Initial™ Ti Bleach Dentin white, BLD-2, 20g
ENTERNAL FEEDING TUBE SILICONE-EF401, 402 & 403
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
FLEXXR* CPM SYSTEM
FDA 510(k)
FDA Class 1
·Physical Medicine
EEA 31 CIRCULAR STAPLER
FDA Adverse Event
Injury
·COVIDIEN·Product code GDW·June 11, 2014
PUMP MMT-522CAS PRDGM INS V2.2 SK EN PR
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·October 14, 2010
OMEGA21 SELFTAPPING SCREW 6 35X50MM
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code MNI·December 14, 2012
SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX
FDA Enforcement
Class II
·Completed·Townsend Design·January 17, 2024