510(k) Report

FDA applicant

The Tiggs Co.

Mchenry, IL1 decision1981–19810 recalls

FDA records 1 decision for The Tiggs Co. (Mchenry, IL) in 1981: 1 510(k) clearance. All are in product code IPW (Orthosis, Sacroiliac, Soft). 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 Tiggs Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Tiggs Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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