FDA applicant

Henry Enterprises, Inc.

Concordia, KS1 decision1990–19900 recalls

FDA records 1 decision for Henry Enterprises, Inc. (Concordia, KS) in 1990: 1 510(k) clearance. All are in product code FNG (Lift, Patient, Ac-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, general hospital panel, where it files most

How often FDA has decided Henry Enterprises, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Henry Enterprises, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Henry Enterprises, 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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Other applicant names beginning “Henry”

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

Henry Schein, Inc. 8 The Henry G. Dietz Co., Inc. 2 Henry Ford Hospital 1

Henry Enterprises, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Henry”