8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
QUINTON MEDTRACK CR PLUS TREADMILL
FDA 510(k)
FDA Class 2
·Physical Medicine
AETOS Shoulder System
FDA UDI
Smith & Nephew, Inc.·00885556867419·HUMERAL HEAD REMOVAL TOOL
XmaruView V1 (Xmaru Chiroview, Xmaru Podview)
FDA 510(k)
FDA Class 2
·Radiology
NEUROCALM MODEL 1 AND 2
FDA 510(k)
FDA Class 2
·Neurology
PROSTHESIS, HIP, SEMI-CONSTRAINED, UNCEMENTED, METAL/POLYMER, NON-POROUS, CALICU
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MEH·October 15, 2025
PFC SIGMARP STB TB IN 2.5 15.0
FDA Adverse Event
Injury
·9616671 DEPUY (IRELAND)·Product code NJL·March 6, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011
EVERA S VR
FDA Adverse Event
Malfunction
·IPG MFG SWITZERLAND·Product code LWS·August 8, 2014