FDA applicant

Tri-Tech, Inc.

Fort Woth, TX11 decisions1981–19970 recalls

FDA records 11 decisions for Tri-Tech, Inc. (Fort Woth, TX) from 1981 to 1997: 11 510(k) clearances. Most are in product codes ISD (Exerciser, Measuring) and JKA (Tubes, Vials, Systems, Serum Separators, Blood…). 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 Tri-Tech, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tri-Tech, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Tri-Tech, Inc.

Which product codes does it file in?

What has FDA decided for it lately?