FDA applicant
Neuro Navigational Corp.
FDA records 23 decisions for Neuro Navigational Corp. (Costa Mesa, CA) from 1993 to 1997: 23 510(k) clearances. Most are in product codes GWG (Endoscope, Neurological) and HRX (Arthroscope). 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 Navigational Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Neuro Navigational Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Neuro Navigational Corp.’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.