FDA applicant

Thor Intl.

Houston, TX2 decisions2003–20040 recalls

FDA records 2 decisions for Thor Intl. (Houston, TX) from 2003 to 2004: 2 510(k) clearances. Most are in product codes ILY (Lamp, Infrared, Therapeutic Heating) and NHN (Powered Light Based Laser Non-Thermal…). Its devices cite 3 predicates, 0 of them its own earlier devices. 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 Thor Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Thor Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Thor”

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

Thor International 1 Thor Medical Instruments, Inc. 1

Thor Intl.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Thor”