FDA applicant

The Henry G. Dietz Co., Inc.

Long Island City, NY2 decisions1991–19940 recalls

FDA records 2 decisions for The Henry G. Dietz Co., Inc. (Long Island City, NY) from 1991 to 1994: 2 510(k) clearances. Most are in product codes NFB (Conserver, Oxygen) and KPR (System, X-Ray, Stationary). 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, anesthesiology panel, where it files most

How often FDA has decided The Henry G. Dietz Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Henry G. Dietz Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Henry G. Dietz Co., 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 “The”

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

Henry Schein, Inc. 8 Henry Enterprises, Inc. 1 Henry Ford Hospital 1

The Henry G. Dietz Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”