FDA applicant

The Spritz Co.

Houston, TX1 decision1991–19910 recalls

FDA records 1 decision for The Spritz Co. (Houston, TX) in 1991: 1 510(k) clearance. All are in product code KTC (Bath, Sitz, Nonpowered). 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, physical medicine panel, where it files most

How often FDA has decided The Spritz Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Spritz Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Spritz Co.’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

The Spritz Co.

Which product codes does it file in?

What has FDA decided for it lately?