FDA applicant

Flow X-Ray Corp.

Great Neck, NY2 decisions1979–20050 recalls

FDA records 2 decisions for Flow X-Ray Corp. (Great Neck, NY) from 1979 to 2005: 2 510(k) clearances. Most are in product codes EAP (Unit, X-Ray, Intraoral) and KPY (Shield, Protective, Personnel). Its devices cite 1 predicate, 0 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, dental panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Flow”

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

Flow Laboratories, Inc. 58 Flow-Fx, LLC 4 Flow Neuroscience AB 1 Flow Cytometry Standards Corp. 1

Flow X-Ray Corp.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Flow”