FDA applicant

Bennett X-Ray Corp.

Copiague, NY23 decisions1977–19970 recalls

FDA records 23 decisions for Bennett X-Ray Corp. (Copiague, NY) from 1977 to 1997: 23 510(k) clearances. Most are in product codes IZH (System, X-Ray, Mammographic) and IZO (Generator, High-Voltage, X-Ray, Diagnostic). Its devices cite 1 predicate, 1 of them its own earlier devices. 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, radiology panel, where it files most

How often FDA has decided Bennett X-Ray Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bennett X-Ray Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bennett X-Ray Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Bennett X-Ray Corp.’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 “Bennett”

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

Bennett X-Ray Technologies 2 Bennett Jacoby, Dds, Ms, Inc. 1 Bennett and Assoc., Inc. 1 Bennett Ergonomic Labs, Inc. 1

Bennett X-Ray Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Bennett”