FDA applicant

Teftec Corp.

Spring Branch, TX8 decisions1996–20020 recalls

FDA records 8 decisions for Teftec Corp. (Spring Branch, TX) from 1996 to 2002: 8 510(k) clearances. All are in product code ITI (Wheelchair, Powered). 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 Teftec Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Teftec Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Teftec Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?