7 results
·
30ms
·
Sources: EU EUDAMED, US FDA
Argen Clear Aligner, Argen Clear Aligner Premium
FDA 510(k)
FDA Class 2
·Dental
BINAXNOW COVID-19 ANTIGEN SELF-TEST
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·June 8, 2022
PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
AIRVO SERIES HUMIDIFIERS
FDA 510(k)
FDA Class 2
·Anesthesiology
BIONIX BLUE 14-16 FRENCH
FDA Adverse Event
Injury
·BIONIX·Product code KNT·October 16, 2014
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 27, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 25, 2011