8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
DENTA PLAST
FDA 510(k)
FDA Class 2
·Dental
UniTip Catheter
FDA UDI
Unisensor AG·07640172971666·
Xpert® Xpress CoV-2 plus
FDA 510(k)
FDA Class 2
·Microbiology
OASYS-ORAL AIRWAY SYSTEM
FDA 510(k)
FDA Class 2
·Dental
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·May 14, 2014
IN TOUCH ZU
FDA Adverse Event
Malfunction
·FLEXTRONICS EMS CANADA·Product code FNL·October 10, 2012
DURATA STS OPTIM ACTIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010
BIOMET StageOne Knee Femoral Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 432170.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020