FDA applicant
Mag & More GmbH
FDA records 5 decisions for Mag & More GmbH (Munich, DE) from 2018 to 2026: 5 510(k) clearances. All are in product code OBP (Transcranial Magnetic Stimulator). Since 2016 its 510(k)s took a median of 268 days from receipt to decision, against 144 for FDA’s reviews in the same codes and years. Its devices cite 13 predicates, 7 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Mag & More GmbH’s devices, and how often a recall has named them.
FDA decisions per year
2in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2018.
Planning a device like Mag & More GmbH’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report