9 results
·
26ms
·
Sources: EU EUDAMED, US FDA
BIOPURE DIALYSATE CONCENTRATE MIX SYST/CONCENTRATE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Nu-Edge Cobalt Chromium Brackets
FDA UDI
TP ORTHODONTICS INC·00192029045503·UL CUS NO HK
PLIF Allograft
FDA UDI
Seaspine Orthopedics Corporation·10889981087913·PLIF Allograft Trial, 9mm x 23mm x 9mm
INTERNATIONAL BIOPHYSICS CORPORATION (IBC) LASER PEEL SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GLUNEO BLOOD GLUCOSE MONITORING SYSTEM, AND PROFESSIONAL BLOOD GLUCOSE MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 22, 2016
LOCKING SCREW
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 25, 2013
COULTER® ACT DIFF2 ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code GKZ·December 16, 2010
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 11, 2014