FDA applicant
Neuro Technology
FDA records 5 decisions for Neuro Technology (Tempe, AZ) from 1982 to 1993: 5 510(k) clearances. Most are in product codes BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)) and BXN (Stimulator, Nerve, Battery-Powered). 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 Neuro Technology’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Neuro Technology since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Neuro Technology’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) ReportOther applicant names beginning “Neuro”
FDA records each applicant name separately; these may or may not be the same firm.