510(k) Report

FDA applicant

U.S. Table, Inc.

Glen Allen, VA5 decisions1995–19950 recalls

FDA records 5 decisions for U.S. Table, Inc. (Glen Allen, VA) in 1995: 5 510(k) clearances. Most are in product codes INQ (Table, Powered) and ITH (Equipment, Traction, 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 U.S. Table, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for U.S. Table, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like U.S. Table, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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