510(k) Report

FDA applicant

Grand Traverse Technologies

Traverse City, MI1 decision1995–19950 recalls

FDA records 1 decision for Grand Traverse Technologies (Traverse City, MI) in 1995: 1 510(k) clearance. All are in product code ILJ (Bath, Hydro-Massage). 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 Grand Traverse Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Grand Traverse Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Grand”

FDA records each applicant name separately; these may or may not be the same firm.