Tonica Elektronik A/S is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Tonica Elektronik A/S - FDA 510(k) Cleared Devices
Recent clearances: MagVenture Accelerated TMS (aTMS) Therapy System, MagVenture TMS Therapy System, MagVenture TMS Therapy System
18
Total
18
Cleared
0
Denied
Tonica Elektronik A/S has 18 FDA 510(k) cleared neurology devices. Based in Farum, DK.
Latest FDA clearance: May 2026. Active since 2006.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MagVenture A/S as regulatory consultant.
FDA 510(k) Regulatory Record - Tonica Elektronik A/S
18 devices
Cleared
May 22, 2026
MagVenture Accelerated TMS (aTMS) Therapy System
Neurology
120d
Cleared
Aug 11, 2025
MagVenture TMS Therapy System
Neurology
122d
Cleared
Aug 08, 2025
MagVenture TMS Therapy System
Neurology
119d
Cleared
Jul 30, 2025
T65 (9016E061-)
Neurology
30d
Cleared
Aug 25, 2023
MagVenture Pain Therapy: MagPro R30, MagPro R30 with MagOption, MagPro X100,...
Physical Medicine
234d
Cleared
Mar 17, 2023
MagVenture TMS Atlas Neuro Navigation System
Neurology
294d
Cleared
Aug 09, 2020
MagVenture TMS Therapy – for treatment of OCD, MagVenture TMS Therapy system
Neurology
286d
Cleared
Aug 14, 2018
Mag Vita TMS Therapy System w/Theta Burst Stimulation
Neurology
265d
Cleared
Oct 05, 2017
MagVita TMS Therapy w/MagPro R20
Neurology
30d
Cleared
Jul 25, 2017
MagVita TMS Therapy System
Neurology
25d
Cleared
Jun 16, 2017
MagVita TMS Therapy System
Neurology
28d
Cleared
May 01, 2017
MagVita TMS Therapy - w/MagPro R20
Neurology
109d