510(k) Report

FDA applicant

Casa Futura Technologies

Monte Sereno, CA1 decision1995–19950 recalls

FDA records 1 decision for Casa Futura Technologies (Monte Sereno, CA) in 1995: 1 510(k) clearance. All are in product code KTH (Device, Anti-Stammering). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ear, nose and throat panel, where it files most

How often FDA has decided Casa Futura Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Casa Futura Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Casa Futura Technologies by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Casa Futura Technologies’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