25 results
·
25ms
·
Sources: EU EUDAMED, US FDA
NORDIC TUMOREX
FDA 510(k)
FDA Class 2
·Radiology
ArgenPMMA 95x25-B1
FDA UDI
ARGEN CORPORATION, THE·D818123306·Crown And Bridge, Temporary, Resin
24M - PG&E Class A 21 BBP
FDA UDI
Certified Safety Manufacturing, Inc.·00766588233062·PG&E Class A 21 BBP - 24M
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981326128·Trial, 14x13mm, 10° Lordosis, 6mm Height, w/o D...
MIRAGE FULL FACE MASK SERIES 2
FDA 510(k)
FDA Class 2
·Anesthesiology
CARDIO 7
FDA 510(k)
FDA Class 2
·Cardiovascular
BD INTRAOSSEOUS NEEDLE SET KIT 25MM
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD) -3006260740·Product code FMI·March 19, 2021
BD INTRAOSSEOUS NEEDLE SET KIT 25MM
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD) -3006260740·Product code FMI·March 19, 2021
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·January 15, 2016
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
TI PANGEA(TM) LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES USA·Product code NKB·May 21, 2013
ADJ PIN COLLET 2.0-3.2MM
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·June 8, 2011
VERSACARE BED
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 20, 2008
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 15, 2013
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 17, 2014