FDA applicant

Bennett X-Ray Technologies

Copiague, NY2 decisions1992–19940 recalls

FDA records 2 decisions for Bennett X-Ray Technologies (Copiague, NY) from 1992 to 1994: 2 510(k) clearances. Most are in product codes IZH (System, X-Ray, Mammographic) and JAC (System, X-Ray, Film Marking, Radiographic). 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 Technologies’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Bennett X-Ray Technologies’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 “Bennett”

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

Bennett X-Ray Corp. 23 Bennett Jacoby, Dds, Ms, Inc. 1 Bennett and Assoc., Inc. 1 Bennett Ergonomic Labs, Inc. 1

Bennett X-Ray Technologies

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bennett”