FDA applicant

Pillar Technology, Inc.

Neodesha, KS6 decisions1991–20010 recalls

FDA records 6 decisions for Pillar Technology, Inc. (Neodesha, KS) from 1991 to 2001: 6 510(k) clearances. Most are in product codes INI (Vehicle, Motorized 3-Wheeled) and 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 Pillar Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pillar Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pillar Technology, Inc.’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

Other applicant names beginning “Pillar”

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

Pillar Surgical, Inc. 7 Pillar Biosciences 1

Pillar Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pillar”