FDA applicant
La Jolla Technology, Inc.
FDA records 5 decisions for La Jolla Technology, Inc. (San Diego, CA) from 1983 to 1987: 5 510(k) clearances. Most are in product codes GXY (Electrode, Cutaneous) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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 La Jolla Technology, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for La Jolla Technology, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like La Jolla Technology, Inc.’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