8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
SYNTEC TRUE LIGHT ENDOILLUMIINATOR WITH PICK
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DuoFLEX Coil Suite
FDA 510(k)
FDA Class 2
·Radiology
ARTIS ZEE AND ZEEGO
FDA 510(k)
FDA Class 2
·Radiology
I-STAT CHEM8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code JGS·November 21, 2017
LIGATING DEVICE
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code MND·June 6, 2014
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·February 21, 2013
OT PING METER
FDA Adverse Event
Malfunction
·Product code NBW·January 28, 2011
BIOMET StageOne Knee Tibial Cement Spacer Mold, 80 MM, Silicone, Sterile, Item 433180.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020