Synaptive Medical, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Synaptive Medical, Inc. has 10 FDA 510(k) cleared medical devices. Based in Toronto On, CA.
Latest FDA clearance: Mar 2024. Active since 2014. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Synaptive Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Synaptive Medical, Inc.
10 devices
Cleared
Mar 25, 2024
Modus IR
Neurology
264d
Cleared
Oct 11, 2023
Synq Software Version 1.3
Radiology
20d
Cleared
Apr 29, 2020
Evry
Radiology
79d
Cleared
Jul 14, 2019
Modus Nav
Neurology
226d
Cleared
Mar 09, 2018
BrightMatter Plan 1.6.0
Radiology
24d
Cleared
Jun 24, 2016
BrightMatter Guide with BrightMatter Pointer
Neurology
120d
Cleared
Mar 30, 2016
BrightMatter Guide with Surface Trace Registration
Neurology
139d
Cleared
Mar 29, 2016
Synaptive ImageDrive Pro
Radiology
138d
Cleared
Apr 02, 2015
BRIGHTMATTER NAVIGATION SYSTEM
Neurology
251d
Cleared
Jun 02, 2014
BRIGHTMATTER PLANNING SOFTWARE
Radiology
112d