FDA applicant

Bardon Ent., Inc.

Hampton, VA1 decision1994–19940 recalls

FDA records 1 decision for Bardon Ent., Inc. (Hampton, VA) in 1994: 1 510(k) clearance. All are in product code JFA (Exerciser, Finger, 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 Bardon Ent., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bardon Ent., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Bardon Ent., 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

Bardon Ent., Inc.

Which product codes does it file in?

What has FDA decided for it lately?