8 results
·
34ms
·
Sources: EU EUDAMED, US FDA
THE NEW 1600 ELECTRODE
FDA 510(k)
FDA Class 2
·Cardiovascular
ERA® Implant Abutment Micro Ang. Base, 2mm Cuff (B)
FDA UDI
STERNGOLD DENTAL LLC·00841549105487·Implant retained overdentures are an establishe...
Integra Salto Total Ankle System
FDA 510(k)
FDA Class 2
·Orthopedic
THERMO TRACE AMMONIA STANDARDS SET, MODELS TR-609
FDA 510(k)
FDA Class 2
·Clinical Chemistry
HOFF PASS-LONG
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF·Product code GYK·May 15, 2014
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·October 31, 2012
GPS PROCEDURAL STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FPO·August 12, 2010
3.2MM GUIDE WIRE 400MM
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·May 4, 2020