Spes Medica Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Spes Medica Srl - FDA 510(k) Cleared Devices
Recent clearances: Subdural Electrode, Strip/Intraoperative Strip, Grid/Intraoperative Grid, Multi-Strip and Split Grid, Intraoperative Mapping Grid, AC Cream - Conductive paste, SAC2 - Electrode Cream
9
Total
9
Cleared
0
Denied
Spes Medica Srl has 9 FDA 510(k) cleared medical devices. Based in Battipaglia, IT.
Last cleared in 2022. Active since 2009. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Spes Medica Srl Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spes Medica Srl
9 devices
Cleared
Nov 10, 2022
Subdural Electrode, Strip/Intraoperative Strip, Grid/Intraoperative Grid,...
Neurology
505d
Cleared
Dec 01, 2021
AC Cream - Conductive paste
Neurology
128d
Cleared
Jan 17, 2020
SAC2 - Electrode Cream
Neurology
119d
Cleared
Nov 22, 2019
Spes Medica Subdermal Needle Electrodes
Neurology
63d
Cleared
Jul 19, 2019
Tech Dots - Adhesive and conductive gel
Neurology
190d
Cleared
Nov 21, 2014
STIM PROBE
Ear, Nose, Throat
387d
Cleared
Jun 11, 2012
DISPOSABLE ADHESIVE SURFACE ELECTRODE
Neurology
115d
Cleared
Aug 24, 2010
LARYNGEAL SURFACE ELECTRODE
Ear, Nose, Throat
299d
Cleared
Aug 11, 2009
DISPOSABLE EMG NEEDLE ELECTRODES, MYOLINE, MYOLINE 2, MYOBOT,
Neurology
90d