FDA applicant

Spectris Technologies, Inc.

Rockford, TN1 decision2004–20040 recalls

FDA records 1 decision for Spectris Technologies, Inc. (Rockford, TN) in 2004: 1 510(k) clearance. All are in product code IOR (Wheelchair, Mechanical). 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 Spectris Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Spectris Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Spectris Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?