9 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR
FDA 510(k)
FDA Class 2
·Physical Medicine
GC Initial™
FDA UDI
Gc America Inc.·15400556704940·GC Initial™ AL Shoulder Transpa ST-31, 20g
GC Initial™
FDA UDI
Gc America Inc.·J0228740761·GC Initial™ Ti Translucent Mod. TM-03, 20g
PROTECT DROPS/SAME AS K874070
FDA 510(k)
FDA Class 2
·Dental
ELECTRO-NERVE STIMULATOR B5/SK700B
FDA 510(k)
FDA Class 2
·Neurology
ARTHROSCOPIC LEG HOLDER 434-21
FDA 510(k)
FDA Class 2
·Orthopedic
ACCU-CHEK ® AVIVA COMBO
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·June 16, 2014
M2A-MAGNUM 42-50MM TPR INSRT-3
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·December 14, 2012
TRUERESULT
FDA Adverse Event
Malfunction
·NIPRO DIAGNOSTICS, INC.·Product code NBW·June 25, 2015