FDA applicant
Neuromodulatory Devices & Applications
FDA records 2 decisions for Neuromodulatory Devices & Applications (San Diego, CA) in 2025: 2 510(k) clearances. All are in product code OBP (Transcranial Magnetic Stimulator). Its devices cite 3 predicates, 1 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 Neuromodulatory Devices & Applications’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 2025.
Planning a device like Neuromodulatory Devices & Applications’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