510(k) Report

FDA applicant

Vibra-Trac Industries

Twin Falls, ID1 decision1989–19890 recalls

FDA records 1 decision for Vibra-Trac Industries (Twin Falls, ID) in 1989: 1 510(k) clearance. All are in product code ILZ (Accessories, Traction). 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 Vibra-Trac Industries’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vibra-Trac Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vibra-Trac Industries by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vibra-Trac Industries’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