Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in DenmarkLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Tonica Elektronik with 18 510(k) clearances. The most recent is a 510(k) clearance dated May 22, 2026: MagVenture Accelerated TMS (aTMS) Therapy System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| May 22, 2026 | MagVenture Accelerated TMS (aTMS) Therapy SystemK260189 · OBP | 510(k) clearances |
| Aug 11, 2025 | MagVenture TMS Therapy SystemK251125 · OBP | 510(k) clearances |
| Aug 8, 2025 | MagVenture TMS Therapy SystemK251119 · OBP | 510(k) clearances |
| Jul 30, 2025 | T65 (9016E061-)K252032 · OBP | 510(k) clearances |
| Aug 25, 2023 | MagVenture Pain Therapy: MagPro R30, MagPro R30 with MagOption, MagPro X100, MagPro X100 with MagOptionK230014 · QPL | 510(k) clearances |
| Mar 17, 2023 | MagVenture TMS Atlas Neuro Navigation SystemK221544 · HAW | 510(k) clearances |
| Aug 9, 2020 | MagVenture TMS Therapy – for treatment of OCD, MagVenture TMS Therapy systemK193006 · QCI | 510(k) clearances |
| Aug 14, 2018 | Mag Vita TMS Therapy System w/Theta Burst StimulationK173620 · OBP | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
