Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
The Magstim Company Limited · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K250286 | Rapid2 Magnetic Stimulators (Magstim Rapid2, Magstim Super R | The Magstim Company Limited | 2025-07-03 | 153 | 0 |
| K243869 | Horizon® 3.0 TMS Therapy System (Horizon 3.0 Inspire); Horiz | The Magstim Company Limited | 2025-03-17 | 90 | 0 |
| K241518 | Horizon® 3.0 TMS Therapy System (Horizon 3.0 Inspire); Horiz | The Magstim Company Limited | 2024-08-30 | 93 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda