10 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
XEROSTOM SALIVA SUBSTITUTE GEL
FDA 510(k)
FDA Unclassified
·Unknown
Sonic
FDA UDI
Sonic Innovations, Inc.·05711583025087·BL80 NR, PS MPL BLISS 80
VIOPTIX ODISSEY TISSUE OXIMETER TISSUE OXIMETER, MODEL OXY-2
FDA 510(k)
FDA Class 2
·Cardiovascular
CONCENTRIC BALLOON GUIDE CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
BD INSYTE AUTOG BC BLU 22GA X 1.0IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·February 5, 2024
T7 DRIVER CANN AO
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code LXH·July 14, 2016
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 3, 2013
SYMBIQ DUAL CHANNEL
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·September 26, 2014
CONTOUR TEST STRIPS
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·June 21, 2011
Immutest 5 Pnl Drug Cup w/ Adult -waived, Item No. IMCA-5AB-W
FDA Enforcement
Class III
·Terminated·Ameditech Inc·December 30, 2015