9 results
·
27ms
·
Sources: EU EUDAMED, US FDA
COMFORTRON PT (TENS)
FDA 510(k)
FDA Class 2
·Neurology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756393881·EYE PACK
STERILE LATEX SURGICAL GLOVES (POWDERED) WITH PROTEIN CONTENT LABELING CLAIM (100 MICROGRAMS OR LESS)
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MIGRA TAB, QUICKSPLINT MIGRAINE
FDA 510(k)
FDA Unclassified
·Unknown
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 19, 2020
REJUVANTE STRGHT PRFIT TMZF MOD STEM SIZE 8
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code KWL·January 4, 2013
JETSTREAM G3
FDA Adverse Event
Injury
·PATHWAY MEDICAL TECHNOLOGIES, INC.·Product code MCW·November 24, 2010
DURATA STS OPTIM ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 2, 2014
CD HORIZON ASTUTE SPINAL SYSTEM
FDA Adverse Event
Injury
·MSD DEGGENDORF MFG·Product code NQP·April 16, 2021