11 results
·
19ms
·
Sources: EU EUDAMED, US FDA
PREZA-PAK II, ARTERIAL BLOOD SAMPLING SY
FDA 510(k)
FDA Class 1
·Anesthesiology
Blue Sky Bio Computerized Orthodontic Bracket System
FDA 510(k)
FDA Class 2
·Dental
SterileRight sterilization pouch and roll
FDA 510(k)
FDA Class 2
·General Hospital
DRIVING CAP/THREADED
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·September 3, 2021
DRIVING CAP/THREADED
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·December 4, 2020
JAMSHIDI BONE MARROW TRAY 11G X4 15G ASP
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code KNW·March 12, 2026
REALSEAL
FDA Adverse Event
Injury
·SYBRONENDO·Product code KIF·May 15, 2014
SENSIA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·October 31, 2012
PULSE GENERATOR 102
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·August 17, 2010
DRIVING CAP/THREADED
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code LXH·September 5, 2023
JAMSHIDI BONE MARROW TRAY 11G X4 15G ASP
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code LWE·October 8, 2025